Verathon 0900-4841-xx-60 GLIDESCOPE BFLEX SINGLE‐USE BRONCHOSCOPES WITH GLIDESCOPE VIDEO MONITOR Operations & Maintenance Manua

GLIDERITE

DLT STYLET

Operations & Maintenance Manual

0900-4841 REV-01

GLIDERITE

DLT STYLET

Operations & Maintenance Manual

Effective: June 4, 2020

Caution: Federal (United States) law restricts this

device to sale by or on the order of a physician.

0900-4841 REV-01

CONTACT INFORMATION

To obtain additional information regarding your GlideScope® system or GlideRite DLT Stylet,

please contact Verathon® Customer Careor visit verathon.com/global-support.

Verathon Inc.

20001 North Creek Parkway

Bothell, WA 98011 U.S.A.

Tel: [phone] (US and Canada only)

Tel: [phone]

Fax: [phone]

verathon.com

Verathon Medical (Europe) B.V.

Willem Fenengastraat 13

1096 BL Amsterdam

The Netherlands

Tel: [phone]

Fax : [phone]

Verathon Medical (Canada) ULC

Verathon Medical (Australia) Pty Limited

Within Australia: 1800 613 603 Tel / 1800 657 970 Fax

International: [phone] Tel / [phone] Fax

Copyright © 2020 by Verathon Inc. All rights reserved.

2227 Douglas Road

Burnaby, BC V5C 5A9

Canada

Tel: [phone]

Fax: [phone]

Unit 9, 39 Herbert Street

St Leonards NSW 2065

Australia

GlideScope, the GlideScope symbol, GlideRite, Verathon, and the Verathon Torch symbol are trademarks of Verathon Inc. All other
brand and product names are trademarks or registered trademarks of their respective owners.

Not all Verathon Inc. products shown or described in this manual are available for commercial sale in all countries.

Information in this manual may change at any time without notice. For the most up-to-date information, see the documentation
available at verathon.com/product-documentation

0900-4841 REV-01

TABLE OF CONTENTS

IMPORTANT INFORMATION .................................................................................................................................1

Product Description ............................................................................................................................................1

Statement of Intended Use ..................................................................................................................................1

Statement of Prescription ....................................................................................................................................1

Notice to All Users ..............................................................................................................................................1

Warnings ............................................................................................................................................................ 2

INTRODUCTION ....................................................................................................................................................4

USING THE STYLET ...............................................................................................................................................5

Procedure 1. Use the GlideRite DLT Stylet ...................................................................................................5

REPROCESSING ...................................................................................................................................................... 6

PRODUCT SPECIFICATIONS ................................................................................................................................... 7

Specifications ......................................................................................................................................................7

Dimensions .........................................................................................................................................................7

GLOSSARY .............................................................................................................................................................8

Operations & Maintenance Manual: Table of Contents

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IMPORTANT INFORMATION

PRODUCT DESCRIPTION

The GlideRite® DLT Stylet was designed to help enable the placement of an endotracheal tube (also known
as an ETT or ET tube). The rigidity of this reusable stylet helps the user manipulate the tube as desired for
intubation. The stylet is for use in 6.0 mm and larger double-lumen ventilation tubes.

STATEMENT OF INTENDED USE

To provide support for a double-lumen endotracheal tube during intubation.

STATEMENT OF PRESCRIPTION

Caution: Federal (United States) law restricts this device to sale by or on the order of a physician.

NOTICE TO ALL USERS

Verathon® recommends that all users read this manual before using the GlideRite DLT Stylet. Failure to do
so may result in injury to the patient, may compromise the performance of the stylet, and may void the
warranty. Verathon recommends that new users:

• Obtain instruction from a qualified individual

• Practice using the stylet on a mannequin before clinical use

• Acquire clinical training experience on patients without airway abnormalities

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WARNINGS

Warnings indicate that injury, death, or other serious adverse reactions may result from use or misuse of the
device. Please heed the following warnings.

WARNING

WARNING

WARNING

Do not allow the stylet to advance past the vocal cords; the ventilation tube should be advanced
off the stylet and into the airway. The stylet must not advance into the glottis under any
circumstances.

During use, the stylet should not protrude beyond the end of the endotracheal tube.

Do not use the product if it appears damaged. Inspect the product before each use.

WARNING

This product is not shipped in sterile condition. Clean it, and apply either high-level disinfection
or sterilization, before its first use. Failure to do so increases the risk of infection.

WARNING

The stylet is considered a semi-critical device that may come into contact with the airway. It
must be thoroughly cleaned and undergo high-level disinfection or sterilization after eachuse.

WARNING

Because the product may be contaminated with human blood or body fluids capable of
transmitting pathogens, all cleaning facilities must be in compliance with (U.S.) OSHA Standard
29CFR1910.1030 “Bloodborne Pathogens” or an equivalent standard.

WARNING

This product may only be cleaned, disinfected, or sterilized by using the approved processes
provided in the GlideScope and GlideRite Products Reprocessing Manual (part number
0900-5032). Cleaning, disinfection, and sterilization methods listed are recommended by
Verathon based on efficacy or compatibility with component materials.

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WARNING

To reduce the risk of cytotoxic residual when cleaning with Metrex CaviCide, thoroughly rinse
the component as instructed in the GlideScope and GlideRite Products Reprocessing Manual
(part number 0900-5032).

WARNING

Verathon has conducted no analysis to establish the compatibility of this product with
environments where magnetic resonance imaging (MRI) equipment is installed. Because of this,
the owner of this product must exclude it from any magnetic resonance (MR) environment.

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INTRODUCTION

The GlideRite DLT Stylet is specifically designed to work with GlideScope® video laryngoscopes. The angle of
the GlideRite DLT Stylet complements the unique angle of the GlideScope instrument to help facilitate quick
placement of a DLT endotracheal tube and to help reduce patient trauma.

Figure 1. GlideRite DLT Stylet with adult size blade

FE AT URES

• Provides maneuverability for placement of a double-lumen endotracheal tube.

• The angle of the stylet complements the angle of adult-sized GlideScope blades.

• Rigid stainless-steel material maintains its shape throughout the intubation.

• Length of stylet fits 6.0mm internal diameter (ID) or larger double-lumen endotracheal tubes.

• Tracheal lumen tube pin holds the double-lumen endotracheal tube in place throughout intubation.

• Reusable, after cleaning and either high-level disinfection or sterilization.

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USING THE STYLET

PRocEdURE 1. USE THE GLIdERITE dLT STYLET

Do not bend or attempt to reshape the stylet. The shape of the stylet is designed to complement the curve
of GlideScope® video laryngoscopes.

1. Ensure the stylet has undergone high-level disinfection or sterilization. For more information,
refer to the GlideScope and GlideRite Products Reprocessing Manual, which is available at

verathon.com/product-documentation.

2. Inspect the stylet for damage. If there is any damage, discard it and contact Verathon® Customer Care or
your local representative to order a new stylet.

3. Load the GlideRite DLT Stylet into the double-lumen tube through the bronchial lumen. Do not permit
the stylet to extend past the distal end of the tube.

4. Rotate the double-lumen tube in order to secure the tracheal lumen on the positioning pin. This changes
the natural bend of the tube. The bronchial tip should now aim posteriorly while the tracheal channel is
aimed anteriorly.

Tracheal lumen
positioning pin

Bronchial lumen

Tracheal lum en

Stylet

5. Place the DLT Stylet and tube at the glottic opening with the tracheal lumen facing anteriorly and the
bronchial lumen pointing down the trachea. Retract the stylet 5–6cm (2–3 3/8 in) with the tracheal lumen
facing anteriorly and the bronchial lumen pointing down the trachea as it advances.

6. Completely remove the DLT Stylet and proceed with the intubation using your preferred technique and
experience.

Operations & Maintenance Manual: Using the Stylet

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REPROCESSING

The GlideRite DLT Stylet is a reusable device that requires cleaning and either high-level disinfection or
sterilization prior to first use and between uses. For information about the cleaning, disinfection, and
sterilization requirements for this component, refer to the GlideScope and GlideRite Products Reprocessing
Manual, which is available at verathon.com/product-documentation.

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PRODUCT SPECIFICATIONS

SPECIFICATIONS

Table 1. GlideRite DLT Stylet Specifications

GENERAL SPECIFICATIONS

Expected product life: 100cycles

Temperature: 10–40°C (50 –10 4°F)

Operating conditions:

Shipping and storage conditions:

DIMENSIONS

Table 2. GlideRite DLT Stylet Dimensions

Relative humidity: 10–95%

Atmospheric pressure: 700–1060 hPa

Temperature: -20– 45°C (-4–113°F)

Relative humidity: 10–95%

Atmospheric pressure: 440 –1060 hPa

GLIDERITE RIGID STYLET (0803‑0009)

Specification Value

Handle width (A) 40 mm (1.6 in)

Handle length (B) 31 mm (1.2 in)

Stylet rod length (C) 394 mm (15.5 in)

Distal tip diameter (D) 5 mm (0.2 in)

A

B

C

Operations & Maintenance Manual: Product Specifications

D

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GLOSSARY

The following table provides definitions for specialized terms used in this manual or on the product itself. For
a full list of caution, warning, and informational symbols used on this and other Verathon® products, please
refer to the Verathon Symbol Directory at verathon.com/symbols.

TERM DEFINITION

AER Automated endoscope reprocessor

C Celsius

CFR Code of Federal Regulations (U.S.)

cm Centimeter

CSA Canadian Standards Association

ETT Endotracheal tube

F Fahrenheit

hPa Hectopascal

ID Internal diameter

in Inch

L Liter

mL Milliliter

mm Millimeter

OSHA Occupational Safety and Health Administration (federal agency in U.S.)

Purewater

Water that is suitable for high-level disinfection according to local regulations
and your medical facility

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