Medtronic VLFT10GEN Instructions for Use
User’s Guide
TM
Valleylab
FT Series Energy Platform
FT10
User’s Guide
ValleylabTM FT10
FT Series Energy Platform
For use with software version 4.0x
Part Number: PT00093618
Preface
Preface
This guide and the equipment it describes are for use only by qualified medical professionals
trained in the particular technique and surgical procedure to be performed. It is intended as
a guide for using the Covidien Valleylab™ FT10 FT Series energy platform (VLFT10GEN) only.
Additional technical information, such as circuit diagrams, component part lists,
descriptions, calibration instructions, component-replacement instructions, and softwareupdate instructions, is available in the Valleylab™ FT10 Energy Platform service manual.
Equipment covered in this manual
Valleylab™ FT10 FT Series Energy Platform (VLFT10GEN) with software version 4.0x
The latest versions of the FT10 user’s guide and the service manual are available at:
https://quickassist.medtronic.com.
Call these numbers to request a hardcopy of the service manual:
• USA and Canada: 1 800 255 8522 Option 2
• International: 1 303 476 7996
ii Valleylab™ FT10 Energy Platform User's Guide
Limited Warranty
Covidien warrants the covered product listed below to be free from defects in material and
workmanship for normal use and service for the period(s) set forth below. Covidien’s
obligation under this warranty is limited to the repair or replacement, at its sole option, of
any product, or part thereof, which has been returned to it (or its authorized distributor)
within the applicable time period shown below after delivery of the product to the original
purchaser, and which examination discloses, to Covidien’s satisfaction, that the product is
defective. This limited warranty does not apply to any product, or part thereof, which has
been repaired or altered in a way so as, in Covidien’s judgment, to affect its stability or
reliability, or which has been subjected to misuse, neglect, or accident.
The warranty period for this Covidien product is as follows:
Limited Warranty
Valleylab™ FT10 FT Series Energy Platform
Notwithstanding any other provision herein or in any other document or communication,
Covidien’s liability with respect to this limited warranty and the products sold hereunder
shall be limited to the aggregate purchase price for the products sold to the customer. This
limited warranty is non-transferable and runs only to the original purchaser of the covered
product(s). There are no warranties which extend beyond the terms hereof. Covidien
disclaims any liability hereunder or elsewhere in connection with the sale of products and
for any form of indirect, tort, or consequential damages.
This limited warranty and the rights and obligations hereunder shall be construed under and
governed by the laws of the State of Colorado, USA. The sole forum for resolving disputes
arising under or relating in any way to this limited warranty is the District Court of the County
of Boulder, State of Colorado, USA.
Covidien reserves the right to make changes in covered products built or sold by it at any
time without incurring any obligation to make the same or similar changes to equipment
previously built or sold by it.
THE OBLIGATION TO REPAIR OR REPLACE A DEFECTIVE OR NONPERFORMING PRODUCT IS
THE SOLE REMEDY OF THE CUSTOMER UNDER THIS LIMITED WARRANTY. EXCEPT AS
EXPRESSLY PROVIDED HEREIN, COVIDIEN DISCLAIMS ALL OTHER WARRANTIES,
WHETHER EXPRESS OR IMPLIED, ORAL OR WRITTEN, WITH RESPECT TO PRODUCTS,
INCLUDING WITHOUT LIMITATION ALL IMPLIED WARRANTIES, WARRANTIES OF
MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE.
One year from date of shipping
Valleylab™ FT10 Energy Platform User's Guide iii
Software License
Software License
Customer hereby acknowledges that Covidien LP and or its affiliates (collectively called
“COVIDIEN” herein) owns the entire right, title, and interest in and to the Software, as may be
installed in the Products or Equipment addressed herein or provided separately (“Software”)
(including all of the computer code, source and object, comprising the Software and all
components and elements thereof), and all associated manuals, drawings, technical
information and Documentation (collectively, the “Documentation”), including, without
limitation, all patent, copyright, trademark, trade secret and other intellectual property or
proprietary rights (“Intellectual Property Rights”) in and to the Software and all components
and elements thereof all of which shall remain the sole and exclusive property of Covidien.
The amount paid by the Customer for the Products and/or Equipment incorporating the
Software includes as a portion of that amount, a license fee granting Customer only the
rights set forth in this Software License. This Software License will be superseded by any
express Software agreement between Covidien and Customer The use of term “Product”
herein includes Products and/or Equipment as applicable.
1. Single User License Grant: COVIDIEN grants to Customer a limited, nonexclusive, nonsublicensable, nontransferable and revocable license to use the Software, exclusively at
location identified by Customer on the order form as the ship-to location of the Products,
solely in machine-readable object code form, and only on a single central processing unit
embedded in the Products as provided by COVIDIEN under this agreement, and solely for the
Customer’s internal business purpose in the operation of the Products provided by
COVIDIEN under this agreement. Notwithstanding anything to the contrary contained in this
Agreement, the Software is licensed to be used on only one computing device or Product,
and a valid license must be obtained under this Agreement for each computing device or
Product with which the Software is used or in which the Software is embedded.
2. Restrictions on Use: Except to the extent expressly authorized in these Software License
Terms or by law, Customer shall not and shall not cause any third part to; (i) decompile,
disassemble, or reverse engineer the Software; (ii) modify or create any derivative works
(including, without limitation, translations, transformations, adaptations or other recast or
altered versions) of or based on the Software, or alter the Software in any way; (iii) merge the
Software with any other software or product not supplied by Covidien; (iv) use, copy, sell,
sublicense, lease, rent, loan, assign, convey or otherwise transfer the Software except as
expressly authorized by this Agreement; (v) distribute, disclose or allow use of the Software,
in any format, through any timesharing service, service bureau, network or by any other
means, to or by third parties; (vi) remove or modify any copyright, confidential or proprietary
markings, legends or restrictions that are in the Software originally supplied to Customer; or
(vii) violate any obligations with regard to Covidien’s Confidential Information (as defined
below). To the extent that Customer is expressly permitted by applicable mandatory law to
undertake any of the activities listed in the preceding sentence, Customer will not exercise
those rights unless and until Customer has given Covidien not less than 30 days’ prior written
notice of Customer’s intent to exercise any such rights unless an order of a government
agency of competent jurisdiction will not so allow. This License will terminate immediately
upon notice from Covidien if Customer fails to comply with any provision of this License or
any agreement.
3. Reservation of Rights: Notwithstanding anything to the contrary contained in this
Agreement, or any order form, purchase order or agreement between the parties, all rights
not expressly granted by Covidien to Customer are reserved to and retained by Covidien and
iv Valleylab™ FT10 Energy Platform User's Guide
Covidien expressly is not selling, assigning or otherwise transferring to Customer, and
Customer is not purchasing or otherwise acquiring or obtaining, any of Covidien’s
Intellectual Property Rights or other rights in or to the Software or Documentation.
4. Confidentiality: Customer agrees that the Software and the Documentation, and all
components and elements of the Software and Documentation, including, without
limitation, the specific design and structure of individual programs, constitutes confidential
information and trade secrets of Covidien (the “Confidential Information”). Customer agrees
not to disclose, provide, or otherwise make available such Confidential Information,
including, without limitation, any trade secrets or copyrighted material, in any form to any
third party. Customer agrees that it will make the Software available only to those
employees, contractors, or consultants of Customer with a specific need to know, who are
obligated to comply with the restrictions contained in these Software License Terms and to
maintain secrecy of the Software and all other Confidential Information and are properly
trained in its use. Customer is responsible for the compliance of all users of the Software and
Products with these obligations and shall cause all users of the Software and Products to
comply with these obligations. Customer acknowledges that the Software embodies
proprietary trade secrets of Covidien including, without limitation, technical and nontechnical information regarding the Software and the development and manufacture of the
same. Customer hereby agrees to maintain the confidentiality of such trade secrets using at
least as great a degree of care as Customer uses to maintain the confidentiality of its own
most confidential information. Customer shall communicate these obligations to those
employees and agents of Customer who come into contact with the Software, and shall use
its best efforts to ensure their compliance with all confidentiality obligations applicable to
Customer.
Software License
5. Change Orders: Covidien shall have the right, at any time during the Term, by written
request to Customer (an “Update Notice”), to require that Customer return the Products and
Software to Covidien for such periods of time as are required by Covidien (“Update Periods”)
or to allow Covidien to access the Software at the Customer’s location for the purpose of
enabling Covidien to incorporate Software revisions, updates or modifications from time to
time. Upon receipt of an Update Notice, Customer shall return the requested Products and
Software to Covidien at Covidien’s cost and expense, or work with Covidien to find a suitable
time for Covidien to access the Software at the Customer’s location. Customer acknowledges
and agrees that during Update Periods, if the Software must be returned to Covidien, the
Products and Software will be unavailable to Customer and in Covidien’s possession.
Covidien will use reasonable commercial efforts to perform the revisions, updates or
modifications and to return the revised, updated or modified Products and Software to
Customer as soon as is reasonably practicable.
6. Software License Term: The term of the Software license granted under this Software
License shall be for the commercial life of the associated Product or Equipment.
7. Limited Warranty: Covidien represents and warrants to Customer that the Software will
perform substantially as described in Covidien's then current Documentation for such
Software and the remaining warranty, or extended warranty, if any, applicable to the Product
or Equipment with which such Software was delivered. If Customer notifies Covidien of
defects during the applicable warranty period, and those defects are verified by Covidien, as
Customer’s sole and exclusive remedy, Covidien will replace the defective Software or, at its
option, terminate this Software License and refund to Customer the amount paid by
Customer to Covidien for the Software (if provided separately from a Product) or for the
Valleylab™ FT10 Energy Platform User's Guide v
Software License
Product in which the defective Software is installed (if embedded within a Product).
Customer’s remedy for breach of this limited warranty shall be limited to the foregoing
replacement or refund and shall not encompass any other damages. No dealer, distributor,
agent or employee of Covidien is authorized to make any modification or addition to the
warranty and remedies stated herein.
Notwithstanding these limited warranty provisions, all of Covidien’s obligations with respect
to such warranties shall be contingent on Customer’s use of the Software in accordance with
this Agreement and in accordance with Covidien’s instructions as provided by Covidien in
the Documentation provided by Covidien, as such instructions may be amended,
supplemented, or modified by Covidien, in its sole discretion, from time to time. Covidien
shall have no warranty obligations with respect to any failures of the Software that are the
result of accident, abuse, misapplication, extreme power surge or extreme electromagnetic
field, or any other cause outside of Covidien’s control.
This limited warranty does not apply to any damages, malfunctions, or non-conformities
caused to or by; (i) Customer’s use of Software in violation of these Software License Terms
or in a manner inconsistent with any Documentation or instructions provided by Covidien;
(ii) use of non-Covidien furnished equipment, software, or facilities with its equipment or
Products; (iii) Customer’s failure to follow Covidien’s installation, operation, repair or
maintenance instructions; (iv) Customer’s failure to permit Covidien timely access, remote or
otherwise, to Products; (v) failure to implement all features, revisions, modifications,
updates, patches, “bug fixes”, or new versions of or to the Software provided by Covidien
under this Agreement or otherwise; (vi) Products with there original manufacturer’s serial
numbers altered, defaced or deleted; (vii) Products that been altered, serviced or modified
by a party other than Covidien; or (viii) Software that has been subjected to abnormal
physical or electrical stress, misuse, negligence or accident by Customer or a third party.
8. Export Laws: THESE SOFTWARE TERMS ARE EXPRESSLY MADE SUBJECT TO ANY AND ALL
LAWS, REGULATIONS, ORDERS, OR OTHER RESTRICTIONS WITH RESPECT TO THE EXPORT
FROM THE UNITED STATES OF AMERICA OF THE SOFTWARE. BUYER SHALL NOT EXPORT OR
RE-EXPORT THE SOFTWARE (I) WITHOUT FULL COMPLIANCE WITH SUCH LAWS,
REGULATIONS, ORDERS AND OTHER RESTRICTIONS, INCLUDING, WITHOUT LIMITATION,
OBTAINING ALL NECESSARY APPROVAL FROM ALL REQUIRED GOVERNMENTAL AGENCIES
AND (II) WITHOUT THE PRIOR WRITTEN CONSENT OF COVIDIEN.
9. U.S. Government Rights. The Software is a “commercial item” developed exclusively at
private expense, consisting of “commercial computer software” and “commercial computer
software Documentation” as such terms are defined or used in the applicable U.S. acquisition
regulations. The Software is licensed hereunder (i) only as a commercial item and (ii) with
only those rights as are granted to all other customers pursuant to the terms and conditions
of this License. Customer shall not use, duplicate, or disclose the Software in any way not
specifically permitted by this License. Nothing in this License requires Covidien to produce
or furnish technical data for or to Customer.
10. Survival. Sections 2, 3, 4, 8, 9 and this Section 10 shall survive the termination or
expiration of these Software License Terms.
vi Valleylab™ FT10 Energy Platform User's Guide
Table of Contents
Preface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ii
Equipment covered in this manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ii
Limited Warranty . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . iii
Software License. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . iv
Chapter 1. Overview and General Features
The Valleylab™ FT10 Energy Platform . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2
Front Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3
Rear Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-4
Modes & Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-5
System Conventions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-16
Touchscreen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-16
System Buttons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-18
Interface Conventions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-19
Chapter 2. Warnings and Precautions for Patient and
Operating Room Safety
Conventions Used in this Guide . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-1
General Warnings and Precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-2
Fire/Explosion Hazards . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-2
System Setup Warnings and Precautions. . . . . . . . . . . . . . . . . . . . . . . . 2-3
Warnings and Precautions for the Energy Platform . . . . . . . . . . . . . . 2-6
Warnings and Precautions for Active Instruments . . . . . . . . . . . . . . . 2-7
Warnings for Implanted Electronic Devices (IEDs) . . . . . . . . . . . . . . . 2-8
Post Surgery Safety Issues . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-9
Warnings and Precautions for Monopolar Procedures . . . . . . . . . . . . . . . . . 2-9
Warnings and Precautions for Patient Return Electrodes. . . . . . . .2-10
Inadvertent Radio Frequency (RF) Burns . . . . . . . . . . . . . . . . . . . . . . .2-11
Warnings and Precautions for Laparoscopic Procedures. . . . . . . . . . . . . .2-13
Warnings and Precautions for Bipolar Procedures . . . . . . . . . . . . . . . . . . . .2-14
Warnings and Precautions for LigaSure™ Technology Procedures. . . . .2-14
Warnings and Precautions for Bipolar Resection . . . . . . . . . . . . . . . . . . . . .2-15
Warnings and Precautions for Cardioblate™ Ablation Procedures . . . . . 2-15
Contraindications for the Cardioblate™ Ablation System . . . . . . .2-15
Cardioblate™ Ablation System Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-18
Cardioblate™ Ablation System Adverse Events . . . . . . . . . . . . . . . . . . . . . . .2-19
Shunt Cords . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-19
Valleylab™ FT10 Energy Platform User’s Guide vii
Conductive Fluid In the Surgical Site. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-19
Servicing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-20
Chapter 3. System Setup
Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2
Unpacking the System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2
Before Starting the System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2
Turning On the Valleylab™ FT10 Energy Platform. . . . . . . . . . . . . . . . 3-3
Turning Off the Valleylab™ FT10 Energy Platform . . . . . . . . . . . . . . . 3-3
Saved Settings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4
Selecting and Editing a Group . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
Renaming a Group . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-7
Deleting Groups . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-7
Favorite Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-9
Favorite Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-9
Adding a Favorite . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-10
Editing a Favorite . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-12
Renaming a Favorite . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-13
Deleting a Favorite . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-13
Recent Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-14
System Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-15
On/Off . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-15
Restore Settings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-15
Audio Volume . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-16
Service and Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-17
Service and Settings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-17
Logs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-18
DEMO Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-19
System Menu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-20
Service Menu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-21
Language Selection Menu. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-21
Chapter 4. Monopolar
Front Panel Monopolar Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-2
Rear Panel Monopolar Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3
Monopolar Quick Setup Instructions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-4
Monopolar Function Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5
Monopolar Power Output Modes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5
Foot Pedal. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5
Monopolar Foot-Pedal Activation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-6
Return Electrodes – REM™ Contact Quality Monitoring System . . . . . . . . 4-6
Patient Return Electrode Considerations . . . . . . . . . . . . . . . . . . . . . . . . 4-7
viii Valleylab™ FT10 Energy Platform User’s Guide
How the REM™ System Works . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-7
Patient Return Electrode Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-8
Monopolar Electrodes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-10
Monopolar Mode Settings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-10
VALLEYLAB™ Mode Functionality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-12
Using a VALLEYLAB-Mode Instrument . . . . . . . . . . . . . . . . . . . . . . . . .4-13
SHARED COAG Functionality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-14
Closing Monopolar Settings Window . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-16
After Surgery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-17
Disconnect the instruments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-17
Chapter 5. Bipolar
Front Panel Bipolar Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-2
Rear Panel Bipolar Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-2
Bipolar Quick Setup Instructions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
Bipolar Function Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
Bipolar Power Output Modes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
Bipolar Default Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4
Foot Pedal. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4
Virtual Ammeter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5
Setting the Ammeter. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5
Auto Bipolar Function. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-6
Turning Auto Bipolar ON/OFF . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-6
Auto Bipolar Activation Impedance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-7
Setting the Auto Bipolar Activation Delay . . . . . . . . . . . . . . . . . . . . . . . 5-7
Closing the Bipolar Settings Window . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-8
Bipolar Adapter. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-8
After Surgery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-9
Disconnect the instruments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-9
Chapter 6. LigaSure™ Technology
Front Panel LigaSure™ Technology Features . . . . . . . . . . . . . . . . . . . . . . . . . . 6-2
Rear Panel LigaSure™ Technology Features . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-2
LigaSure™ Technology Quick Setup Instructions . . . . . . . . . . . . . . . . . . . . . . 6-3
LigaSure™ Technology Function Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-4
LigaSure™ Technology Default Settings . . . . . . . . . . . . . . . . . . . . . . . . . 6-5
LigaSure™ Technology/Bipolar Receptacle . . . . . . . . . . . . . . . . . . . . . . 6-5
Foot Pedal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-6
LigaSure™ Technology Instruments. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-6
Reusable-Instrument Assembly. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-6
Valleylab™ FT10 Energy Platform User’s Guide ix
Connecting LigaSure™ Technology Instruments
to the Energy Platform . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-6
Activating the LigaSure™ Technology Instrument . . . . . . . . . . . . . . . . . . . .6-10
Alert Situations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-10
BiZact™ Function Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-12
After Surgery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-13
Disconnect the instruments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-13
Chapter 7. Bipolar Resection
Front Panel Bipolar Resection Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-2
Rear Panel Bipolar Resection Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-2
Bipolar Resection Quick Setup Instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-3
Bipolar Resection Function Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-3
LigaSure™ Technology/Bipolar Receptacle . . . . . . . . . . . . . . . . . . . . . . 7-4
Bipolar Resection Default Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-4
Foot Pedal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-5
Connecting Bipolar Resection Instruments to the VLFT10GEN . . . 7-6
Bipolar Resection Settings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-6
Changing the Energy-Delivery Setting . . . . . . . . . . . . . . . . . . . . . . . . . . 7-6
Activating a Bipolar Resection Instrument . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-7
Incorrect Foot-Pedal Error . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-7
After Surgery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-8
Disconnect the Instruments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-8
Chapter 8. Cardioblate™ Surgical Ablation System
Front Panel Cardioblate™ Ablation Features . . . . . . . . . . . . . . . . . . . . . . . . . . 8-2
Rear Panel Cardioblate™ Ablation Features . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-2
Cardioblate™ Ablation System Quick Setup Instructions. . . . . . . . . . . . . . . 8-3
Cardioblate™ Ablation System Function Overview . . . . . . . . . . . . . . . . . . . . 8-4
Monopolar Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-4
Cardioblate™ Ablation System Default Settings . . . . . . . . . . . . . . . . . . . . . . . 8-5
Cardioblate™ Ablation System Receptacles . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-5
Monopolar 2 Receptacle. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-5
LigaSure™ Technology/Bipolar Receptacle . . . . . . . . . . . . . . . . . . . . . . 8-5
Cardioblate™ Ablation System Single Foot Pedal for Monopolar and
Bipolar . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-6
Cardioblate™ Ablation System Instruments and Devices. . . . . . . . . . . . . . . 8-6
Connecting Monopolar Cardioblate™ Devices
to the Energy Platform . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-6
Connecting Bipolar Cardioblate™ Devices
to the Energy Platform . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-7
x Valleylab™ FT10 Energy Platform User’s Guide
Cardioblate™ Ablation System Monopolar Settings . . . . . . . . . . . . . . . . . . . 8-8
Changing the Cardioblate™ Ablation System
Monopolar Energy-Delivery Setting. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-8
Cardioblate™ Ablation System Bipolar Settings . . . . . . . . . . . . . . . . . . . . . . . 8-9
Switching between Cardioblate™ Ablation System
Monopolar and Bipolar Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-9
Activating a Cardioblate™ Ablation System Monopolar Pen . . . . . . . . . .8-10
Activating a Cardioblate™ Ablation System Bipolar Device . . . . . . . . . . .8-10
Transmurality Indicator for Bipolar Lesions. . . . . . . . . . . . . . . . . . . . . . . . . . . 8-11
Alert Situations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-12
High Impedance Detected. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-12
Low Impedance Detected . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-13
Prolonged Activation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-13
Return Electrode Over-Temperature . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-14
Verification Error . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-14
Cardioblate™ Ablation System Historical Graph Review . . . . . . . . . . . . . .8-15
Cardioblate™ Ablation System Historical Graph Data Export . . . . . . . . . .8-15
After Surgery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-16
Disconnect the instruments/devices . . . . . . . . . . . . . . . . . . . . . . . . . . .8-16
Chapter 9. Troubleshooting
General Troubleshooting Guidelines . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-2
REM Alarms. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-2
Correcting a REM-Alarm Condition. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-2
Correcting Malfunctions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-3
System Errors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-8
Chapter 10. Maintenance and Repair
Responsibility of the Manufacturer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10-2
Routine Maintenance and Periodic Safety Checks . . . . . . . . . . . . . . . . . . . .10-2
Cleaning. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10-3
Product Service . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10-3
Returning the Energy Platform for Service. . . . . . . . . . . . . . . . . . . . . .10-4
Software Updates. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10-4
Updating Energy Platform Software . . . . . . . . . . . . . . . . . . . . . . . . . . .10-5
Service Manual Copies and Updates . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10-6
Covidien Technical Service . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10-6
Training/Education . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-6
Chapter 11. Technical Specifications
Valleylab™ FT10 Energy Platform Specifications . . . . . . . . . . . . . . . . . . . . . .11-2
Valleylab™ FT10 Energy Platform User’s Guide xi
General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-2
Dimensions and Weight . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-2
Environmental Parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-3
Input Power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-3
Power Cord Specifications. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-4
Backup Power. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-4
Equipotential Ground Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-4
EKG Blanking and Smoke Evacuation . . . . . . . . . . . . . . . . . . . . . . . . . .11-4
Internal Memory . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11-5
Duty Cycle . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-5
Leakage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-5
Radio Frequency Identification (RFID). . . . . . . . . . . . . . . . . . . . . . . . . . 11-6
FCC Statement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11-6
Ethernet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11-7
USB. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11-7
Monopolar 2 Communication . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11-7
Symbols Used . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-7
Standards and IEC Classifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-11
Class I Equipment (IEC 60601-1) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-11
Type CF Equipment/Defibrillator Proof
(IEC 60601-1, IEC 60601-2-2, and ANSI/AAMI HF18) . . . . . . . . . . . .11-11
IP21 Liquid Ingress/Spillage
(IEC 60601-1 and IEC 60601-2-2) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-11
Voltage Transients – Energy Platform Mains Transfer
(IEC 60601-1, IEC 60601-2-2, and ANSI/AAMI HF18) . . . . . . . . . . . .11-11
CISPR 11 Class A. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-12
Electromagnetic Compatibility
(IEC 60601-1-2 and IEC 60601-2-2) . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-12
Return Electrode Monitor (REM) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-12
Auto Bipolar . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-14
Audio Tones . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-15
Displayed Time Accuracy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-17
Energy Output Characteristics. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-17
Output Waveforms. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-19
Output Power vs. Resistance Graphs. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-21
Monopolar Graphs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-21
Bipolar Graphs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-36
Discontinuous Power Curves . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11-52
xii Valleylab™ FT10 Energy Platform User’s Guide
Chapter 1
Overview and General Features
This chapter provides an overview of the features and functions of the Valleylab™ FT10 FT
Series energy platform.
Precaution
Read the instructions, warnings, and precautions provided with this energy platform and associated
accessories before using. Specific instructions for electrosurgical instruments are not included in this
manual.
Valleylab™ FT10 Energy Platform User's Guide 1-1
The Valleylab™ FT10 Energy Platform
The Valleylab™ FT10 Energy Platform
Introduction
The Valleylab™ FT10 FT Series Energy Platform (VLFT10GEN) provides RF energy for
monopolar and bipolar surgical applications, tissue-fusion and vessel-sealing applications,
and cardiac applications. It features a touchscreen divided into four quadrants for viewing
settings, user input of settings, and options available for any application. The energy
platform automatically detects coded handsets and configures the energy platform
accordingly. Safety and diagnostic functionality include automatic fail-safe functions.
The Valleylab™ FT10 Energy Platform, applied parts (patient return electrodes and active
instruments) are designed to work as a system. Covidien offers a selection of patient return
electrodes and active instruments that are fully compatible with this energy platform.
• Refer to each instrument’s instructions for use (IFU) for indications, warnings, and specific
contraindications.
• When considering other manufacturers’ patient return electrodes and/or active
instruments, customers should seek detailed user instructions and warning information
from the manufacturer.
The energy platform is intended for use in general surgery and such surgical specialties as
urologic, vascular, thoracic, plastic, gynecologic, reconstructive, cardiac, and colorectal
surgery.
Indications for Use
The Valleylab™ FT10 Energy Platform is a high frequency electrosurgical generator intended
for use with monopolar and bipolar accessories for cutting and coagulating tissue. When
used with compatible sealing devices, it is indicated for sealing vessels up to and including
7 mm, tissue bundles, and lymphatics. When used with compatible ablation devices it is
indicated for cardiac tissue ablation.
The generator can also be used with compatible resectoscopes for endoscopically controlled
removal or coagulation of tissue using 0.9% NaCl solution as the irrigation medium.
The tissue fusion function has not been shown to be effective for tubal sterilization or tubal
coagulation for sterilization procedures. Do not use this function for these procedures.
Contraindications
The cardiac tissue ablation feature is contraindicated for patients that have active
endocarditis at the time of surgery.
Ablation in a pool of blood is contraindicated (for example, through a purse string suture).
1-2 Valleylab™ FT10 Energy Platform User's Guide
Front Panel
The Valleylab™ FT10 Energy Platform
Overview and General Features
10
FT10
11
1
2
4
3
On/Off button
ཱ Restore Settings button
ི Audio Volume control button
ཱི Service/Settings button
ུ REM™ (Return Electrode Monitoring) indicator
ཱུ Interface touchscreen
ྲྀ REM patient return electrode receptacle
ཷ LigaSure™ technology/Bipolar receptacle
ླྀ Monopolar 2 instrument receptacle
ཹ Monopolar 1 Universal Foot Pedal Port (UFP) receptacle
ེ Bipolar instrument receptacle
9
8
5
6
7
Valleylab™ FT10 Energy Platform User's Guide 1-3
The Valleylab™ FT10 Energy Platform
Rear Panel
1
2
Monopolar 2 Monopolar 1
Bipolar
3
4
5
Warning: Risk of Fire.
Replace Fuse as Marked
250V, F10.0A (100-127Vac)
250V, F6.3A (220-240Vac)
Monopolar1Monopolar
2
Avertissement: Risque du feu.
Remplacez les fusibles
comme marqués.
250V, F10.0A (100-127Vac)
250V, F6.3A (220-240Vac)
10
89
6
7
Monopolar 2 foot-pedal receptacle (requires included adapter to connect standard four-
pin monopolar foot pedal)
ཱ Monopolar 1 foot-pedal receptacle
ི LigaSure™ technology/Bipolar foot-pedal receptacle (requires included adapter to
connect a bipolar resection foot pedal)
ཱི Bipolar foot-pedal receptacle
ུ Fuse drawer
ཱུ Power cord receptacle
ྲྀ Equipotential ground connection
ཷ Service receptacle (Covered. For service only.)
ླྀ Ethernet receptacle (Covered. For service only.)
ཹ Interlink cable receptacles for EKG blanking and smoke-evacuation control
1-4 Valleylab™ FT10 Energy Platform User's Guide
The Valleylab™ FT10 Energy Platform
Modes & Settings
The Valleylab™ FT10 energy platform provides the following modes and settings for a variety
of surgical procedures:
Monopolar modes Power-Setting Ranges Peak Voltage
· CUT
- PURE Off, 1–300 W 1287 V
- BLEND Off, 1–200 W 2178 V
· VALLEYLAB 5–60 W 2783 V
· COAG
Overview and General Features
- SOFT Off, 1–120 W 264 V
- FULGURATE Off, 1–120 W 3448 V
- SHARED
FULGURATE
- SPRAY Off, 1–120 W 3932 V
-SHARED
SPRAY
Bipolar modes
· PRECISE Off, 0.5–70 W 184 V
· STANDARD Off, 1-70 W 415 V
· MACRO Off, 1-70 W 530 V
LigaSure™ technology
(tissue fusion)
Bipolar Resection effects
· CUT 1–6 849 V
Off, 1–120 W 3448 V
Off, 1–120 W 3932 V
No power settings 244 V
· COAG 1–6 318 V
Cardioblate™ Ablation
· Monopolar Off, 1-50 W 382 V
· Bipolar No power Settings 382 V
Valleylab™ FT10 Energy Platform User's Guide 1-5
The Valleylab™ FT10 Energy Platform
Electrosurgical Monopolar Modes
The system produces six modes of monopolar power output for electrosurgery.
Precaution
To provide expected functionality from a hand piece, proper insertion is required. Refer to the
alignment dots below the receptacles for proper insertion orientation.
CUT Modes
• PURE CUT provides a clean, precise cut in any tissue with little or no hemostasis.
• BLEND CUT is a conventional blended waveform that provides slower cutting with
simultaneous hemostasis.
VALLEYLAB™ mode
• VALLEYLAB mode is a unique combination of hemostasis and dissection that allows the
user to slow down for more hemostasis and speed up for faster dissection.
COAG Modes
• SOFT desiccates tissue at a relatively slower rate with deeper thermal penetration. It is
typically performed with a ball electrode and a saline drip.
• FULGURATE coagulates tissue by sparking from the active electrode, through air, to the
patient tissue.
• SPRAY delivers wider fulguration; penetration is shallower and the affected tissue area is
larger than with the FULGURATE mode.
• SHARED allows two monopolar instruments to activate simultaneously in either
FULGURATE or SPRAY modes. A single power setting is provided and power is shared
between the two instruments.
Note: SOFT and SHARED COAG modes are features that are not available on the clinical
screen until they have been enabled. These features can be enabled through Valleylab™
Exchange by a Covidien sales representative.
Compatible Monopolar Instruments & Devices
The following Covidien catalog numbers for monopolar surgical instruments, return
electrodes, foot pedals, and adapters are fully compatible with the Valleylab™ FT10 energy
platform.
Monopolar UFP Instruments (connect only to Monopolar 1)
E05021 Monopolar Adapter
E050212 Monopolar Adapter
The Monopolar 1 UFP-receptacle, identified by a blue ring, accepts UFP connectors with
diameters of 4 mm to 8 mm, and lengths of 15.2 mm to 41.7 mm. UFP connectors with a
diameter of less than 4 mm require an adapter to connect to the Monopolar 1 UFP
receptacle.
1-6 Valleylab™ FT10 Energy Platform User's Guide
The Valleylab™ FT10 Energy Platform
Monopolar Instruments (connect only to Monopolar 2 receptacle)
FT3000DB Force TriVerse™ Electrosurgical Device
FT3000 Force TriVerse™ Electrosurgical Device
Monopolar Instruments (connect to either Monopolar 1 or Monopolar 2)
This energy platform is designed for use with Covidien monopolar instruments. However, other
monopolar instruments are compatible with the Valleylab™ FT10 energy platform if they have a
connector that matches the following figure, are rated for peak voltages of at least 3932 V, and have
a total length no greater than 17 ft (5.2 m).
Monopolar
Overview and General Features
Utilizes 4 mm banana pins
Return Electrodes (Monitoring)
E0560 Valleylab™ REM Patient Return Electrode Cord
E7507 REM Polyhesive™ Adult Patient Return Electrode
E7507DB REM Polyhesive™ Adult Patient Return Electrode
E7508 REM Polyhesive™ Adult Cordless Patient Return Electrode
E7509 REM Polyhesive™ Adult Cordless Patient Return Electrode
E7509B REM Polyhesive™ Adult Cordless Patient Return Electrode
E7510-25 REM Polyhesive™ Infant Patient Return Electrode
E7510-25DB REM Polyhesive™ Infant Patient Return Electrode
E7512 REM Polyhesive™ Neonatal Patient Return Electrode
Valleylab™ FT10 Energy Platform User's Guide 1-7
The Valleylab™ FT10 Energy Platform
Return Electrodes (Non-Monitoring, for use in DEMO mode only. Not for clinical use.)
E7506 Non-REM Polyhesive™ Patient Return Electrode
REM Connector
E0507B Valleylab™ Multiple Return/S Cord Adapter
The Covidien return electrodes have a total length no greater than 16 ft (4.9 m).
Foot Pedals
The Covidien foot pedals have a total length no greater than 16 ft (4.9 m).
FT6003 ForceTriad™ Three-pedal Footswitch (Monopolar 2 only)
E6008 Valleylab™ Monopolar Footswitch (Monopolar 1, Monopolar 2 with adapter)
E6008B Valleylab™ Monopolar Footswitch (Monopolar 1, Monopolar 2 with adapter)
1017577 6-pin to 4-pin Monopolar Footswitch Adapter (Monopolar 2 only)
Bipolar Modes
Selection of bipolar modes and power settings is dependent on surgeon preferences, tissue
characteristics, accessories selection, and the intended clinical application.
PRECISE mode may be used when it is essential to maintain a high degree of precision and
fine control over the amount of desiccation. Voltage is kept low to prevent sparking. Power
remains constant over a specific range of tissue resistance, allowing a consistent tissue effect.
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The Valleylab™ FT10 Energy Platform
STANDARD mode may be used for most bipolar applications. Voltage is kept low to prevent
sparking. Power remains constant over a specific range of tissue resistance, allowing a
consistent tissue effect.
MACRO mode may be used for bipolar cutting or rapid coagulation. Voltage is higher and
there is more power than in the other available bipolar modes.
Overview and General Features
Mode
Setting
PRECISE 0.5—70 watts
STANDARD 1—70 watts • Medium surface-area instruments
MACRO 1—70 watts • Large surface-area instruments
Power Setting Range Optimized Instrumentation
• Small surface-area instruments
(0.5 watt increments
up to 10 watts)
• Micro-tip forceps (0.4—2.2 mm)
• Micro-tip forceps (1.0—2.2 mm)
• Small paddle lap forceps
• Bipolar scissors
• Large paddle lap forceps
Auto Bipolar
The Auto Bipolar feature senses tissue impedance between the two bipolar electrodes, then
uses the impedance information to automatically start or stop bipolar RF energy delivery.
Optionally, the user may select a timed activation delay for auto start of RF activation.
Note: When using Auto Bipolar, the tissue in the grasp of the bipolar device must have an
impedance less than 2200 . The activation impedance safety feature will not deliver RF
power to the tissue if it is not within the specified range. This is a factory-set value that
cannot be reset by the user.
Note: Auto Bipolar is a feature that is not available on the clinical screen until it is enabled.
This feature can be enabled through Valleylab™ Exchange by a Covidien sales representative.
Important
If the VLFT10ADP1 bipolar adapter is used, only one bipolar instrument can set the Auto Bipolar
feature to ON.
Precaution
Do not use instruments with flying leads with the Valleylab™ FT10 energy platform.
Do not use the FT0501 ForceTriad™ bipolar adapter on the Valleylab™ FT10 energy platform.
Compatible Bipolar Instruments & Devices
The Valleylab™ FT10 energy platform is designed for use with Covidien bipolar instruments.
However, other bipolar instruments are compatible with the FT10 if their connectors match
Valleylab™ FT10 Energy Platform User's Guide 1-9
The Valleylab™ FT10 Energy Platform
the following illustration, are rated for peak voltages of at least 531 V, and have a total length
no greater than 16 ft (4.9 m).
Bipolar
Utilizes 4 mm banana pins
Bipolar with Handswitching
A. Utilizes 4 mm banana pins
B. Utilizes 2 mm banana pins
The following Covidien catalog numbers for bipolar foot pedals are fully compatible with the
Valleylab™ FT10 energy platform. They have a total length no greater than 16 ft (4.9 m).
Foot Pedals
E6009 Valleylab™ Bipolar Standard Footswitch
E6009B Valleylab™ Bipolar Standard Footswitch
E6019 Valleylab™ Bipolar Dome Footswitch
Bipolar Adapter
The VLFT10ADP1 Bipolar Adapter allows bipolar instruments to connect to the LigaSure™
technology/Bipolar receptacle, thereby enabling the use of a second bipolar instrument.
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The Valleylab™ FT10 Energy Platform
LigaSure™ Technology
LigaSure™ technology tissue fusion can be used on arteries, veins, pulmonary vasculature,
and lymphatics—up to and including 7 mm in diameter—and tissue bundles. When used
with compatible instruments, the system provides precise energy delivery and electrode
pressure to vessels for a controlled time period to achieve a complete and permanent fusion
of the vessel lumen. The system is designed to produce minimal sticking, charring, and
thermal spread to adjacent tissue.
Warning
The tissue fusion function has not been shown to be effective for tubal sterilization or tubal
coagulation for sterilization procedures. Do not use this function for these procedures.
LigaSure™ Technology Instruments
The LigaSure™ technology instruments that complete the Valleylab™ FT10 energy platform
tissue-fusion system include reusable and single-use instruments for open and laparoscopic
procedures. Each reusable instrument requires a corresponding single-use electrode. The
LigaSure™ technology function is only available when using compatible instruments.
Overview and General Features
Compatible LigaSure™ Technology Instruments & Devices
This energy platform is designed for use with Covidien LigaSure™ technology instruments
that have a connector that matches the following figures, are rated for peak voltages of at
least 244 V, and have a total length no greater than 12.5 ft (3.8 m). However, it does not
recognize all LigaSure™ technology instruments. Please refer to the cover of the instructions
for use to confirm if a specific LigaSure™ technology catalog number is compatible with the
Valleylab™ FT10 energy platform.
LigaSure
Utilizes 4 mm banana pins
Valleylab™ FT10 Energy Platform User's Guide 1-11
The Valleylab™ FT10 Energy Platform
LigaSure with Switching
A. Utilizes 4 mm banana pins
B. Utilizes 2 mm banana pins
A
29,21 mm
44,7 mm
22,4 mm
B
A
A. Utilizes 4 mm banana pins
B. Utilizes 2 mm banana pins
The following LigaSure™ foot pedal is fully compatible with the Valleylab™ FT10 energy
platform. It has a total length no greater than 16 ft (4.9 m).
Foot Pedal
LS0300 Tissue Fusion Footswitch, Purple
Bipolar Resection
Bipolar Resection configures the LigaSure™ technology/Bipolar receptacle to use bipolar
resection resectoscopes. The accessories have a total length no greater than 17 ft (5.2 m).
1-12 Valleylab™ FT10 Energy Platform User's Guide
Accessories
FT0021S ForceTriad™ Bipolar Resection Cord
FT0022W ForceTriad™ Bipolar Resection Cord
FT6009 ForceTriad™ FT Series Bipolar Resection Footswitch (with adapter)
1060355 Valleylab™ FT10 Bipolar Resection Footswitch Adapter
Effect-Settings Reference Chart
The Valleylab™ FT10 Energy Platform
Overview and General Features
Effect
Setting
1 189.5 135 300 25
2 189.5 157 310 50
3 189.5 186 320 75
4 189.5 220 330 100
5 189.5 260 340 125
6 189.5 300 350 150
CUT Initiation
Average Power
(watts)
CUT Therapeutic
Power (watts)
CUT Therapeutic
(max RMS volts)
COAG (max RMS
volts)
Cardioblate™ Ablation System
The Cardioblate™ surgical ablation system is designed to deliver radiofrequency (RF) energy
to selected sites using a Cardioblate™ surgical ablation device.
Note: Cardioblate™ ablation is a feature that is not available on the clinical screen until it has
been enabled. This feature can be enabled through Valleylab™ Exchange by a Covidien sales
representative.
Cardioblate™ Ablation System Instruments and Devices
The Cardioblate™ instruments that allow the cardiac ablation capability include single-use
instruments. Cardioblate™ ablation energy delivery is only available when using compatible
instruments.
Cardioblate™ Ablation System Return Electrodes (Monitoring)
Utilize adult patient return electrodes with Cardioblate™ monopolar.
E7507 REM Polyhesive™ Adult Patient Return Electrode
E7507DB REM Polyhesive™ Adult Patient Return Electrode
E7508 REM Polyhesive™ Adult Cordless Patient Return Electrode
Valleylab™ FT10 Energy Platform User's Guide 1-13
The Valleylab™ FT10 Energy Platform
E7509 REM Polyhesive™ Adult Cordless Patient Return Electrode
E7509B REM Polyhesive™ Adult Cordless Patient Return Electrode
Cardioblate™ Ablation System Monopolar Pens
The energy platform is designed for use with Medtronic Cardioblate™ ablation system
monopolar instruments with a connector that matches the following figure, are rated for
peak voltages of at least 382 V, and have a total length no greater than 17 ft (5.2 m).
Cardioblate™ Ablation System Monopolar Pens
31.7 mm
19 mm
9.6 mm
Cardioblate™ Ablation System Bipolar Instruments and Devices
The energy platform is designed for use with Medtronic Cardioblate™ ablation system
bipolar instruments with a connector that matches the following figure, are rated for peak
voltages of at least 382 V, and have a total length no greater than 17 ft (5.2 m).
Cardioblate™ Ablation System Bipolar Instruments and Devices
A
29,21 mm
44,7 mm
22,4 mm
B
A
A. Utilizes 4 mm banana pins
B. Utilizes 2 mm banana pins
Cardioblate™ Ablation System Monopolar and Bipolar Foot Pedal
LS0300 Tissue Fusion Footswitch, Purple
Connection to External Systems
The Valleylab™ FT10 energy platform can be connected to an external system. For example,
connections can be made to enable smoke evacuation or EKG blanking during monopolar
1-14 Valleylab™ FT10 Energy Platform User's Guide
The Valleylab™ FT10 Energy Platform
activation, or provide argon-enhanced coagulation. Refer to the external system user’s guide
for detailed instructions regarding how to connect it to the energy platform.
There are two external system receptacles on the back of the Valleylab™ FT10 energy
platform that can signal RF activation. The receptacles are labeled Monopolar 1 and
Monopolar 2. The way the receptacles signal RF activation is dependent upon the country
code selection of the energy platform. This is done to meet the smoke evacuation
regulations of each country. Upon setting the country code, one of the following behaviors
will signal RF activation:
• both external system receptacles signal any monopolar RF activation.
• both external system receptacles signal any monopolar or bipolar RF activation.
• both external system receptacles signal any RF activation.
External Systems Compatible with the Valleylab™ FT10 Energy Platform
SEA3730 RapidVac™ Smoke Evacuator Interlink Cable (cable length = 10 ft (3m)
Overview and General Features
SE3690 RapidVac™ Smoke Evacuator
Force™ Argon II-20 Argon Gas Delivery Unit II
Warning
Only medical devices compliant with IEC 60601-1 may be connected to the external system
receptacles. The use of any external system connected to the Valleylab™ FT10 energy platform should
be evaluated by qualified personnel.
Valleylab™ FT10 Energy Platform User's Guide 1-15
System Conventions
System Conventions
Touchscreen
The Valleylab™ FT10 energy platform features a user-friendly touchscreen interface to
control system functions. The touchscreen is divided into quadrants; each of the four
sections is associated with an adjacent instrument receptacle.
• Quadrant 1—Settings entered in the touchscreen control an instrument attached to the
Monopolar 1 receptacle.
• Quadrant 2—Settings entered in the touchscreen control an instrument attached to the
Monopolar 2 receptacle.
• Quadrant 3—Settings entered in the touchscreen control an instrument attached to the
Bipolar receptacle.
• Quadrant 4—The touchscreen displays instrument-specific options and activation of
LigaSure™ technology and bipolar resection devices.
1 2
FT10
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