Display 6-digit
Weighing range (max) 250 kg
Minimum load (Min) 2 kg
Verification value (e) 100 g
Reproducibility 0.1 kg
Linearity ± 0.1 kg
Display LCD with 25mm high digits
Recommended adjustment
weight, (Class)
> 200 kg
(M1)
Stabilization time (typical) 2 sec.
Warm-up time 10 min
Operating temperature 0° C …. + 40° C
Humidity of air max. 80 % (not condensing)
Electric Supply Input voltage 220V-240V AC, 50 Hz
Auto Off After 3 min without load change (adjustable)
Balance
(W x D x H) mm
365 x 450 x 1020
Weighing plate mm 365 x 360 x 80
Weight kg (net) 13 14
Height measuring stick in
tripod integrated, extendable
-
(from 88cm to 200 cm)
Rechargeable battery
operation
optional
Batteries6 x 1.5 V AA
Data interface
provided as standard
4 MPC_M / MPE_HM / MPE_PM-BA-e-1414
RS 232 C
KERN MPC 250K100M
Display 6-digit
Weighing range (max) 250 kg
Minimum load (Min) 2 kg
Verification value (e) 100 g
Reproducibility 0.1 kg
Linearity ± 0.1 kg
Display LCD with 25mm high digits
Recommended adjustment
weight, (Class)
Stabilization time (typical) 2 sec.
Warm-up time 10 min
Operating temperature 0° C …. + 40° C
Humidity of air max. 80 % (not condensing)
Electric Supply Input voltage 220V-240V AC, 50 Hz
Balance
(W x D x H) mm
Weighing plate mm 365 x 360 x 80
Weight kg (net) 8.2
Wall bracket
Rechargeable battery
operation
Batteries6 x 1.5 V AA
(without display unit)
> 200 kg
(M1)
365 x 360 x 80
optional
Data interface
provided as standard
MPC_M / MPE_HM / MPE_PM-BA-e-1414 5
RS 232 C (optional)
This EC verification mark indicates that these scales are in
are approved for medical purposes within the European Union.
Designation of the serial number of every device, applied at the
Number here as example
2015-01
Identification of the manufacturing date of the medical product.
“Please note the accompanying documents“
M
year
2 Declaration of conform ity
Declaration of conformity: see separate document showing serial number of device
CE marking:
2.1 Explanation of the graphic symbols
0297
0103
WF 150012
conformity with EU Directive 2009/23/EG for Non-Automatic
Weighing Instruments.
Hold function/Calculation of a stable weight value
BMI key
Function key
Calculation of the Body Mass Index
In menu:
• Confirm selection
For numeric entry:
• Confirm numerical value
In menu:
• Call up menu
• How to select menu items
For numeric entry:
• Increase numerical value
Zeroing key
TARE key
Weighing scale will be reset to „0.0“
For numeric entry:
• Change decimal place
Tare balance
MPC_M / MPE_HM / MPE_PM-BA-e-1414 11
4.2 MPE models
Key Description Function
ON/OFF-switch Turn on/off
HOLD button
Hold function/Calculation of a stable weight value
BMI key
Calculation of the Body Mass Index
PRINT button
(MPE models only)
Function key
Data transfer via interface
In menu:
• Confirm selection
For numeric entry:
• Confirm numerical value
In menu:
• Call up menu
• How to select menu items
For numeric entry:
• Increase numerical value
Zeroing key
TARE key Tare balance
Weighing scale will be reset to „0.0“
For numeric entry:
• Change decimal place
12 MPC_M / MPE_HM / MPE_PM-BA-e-1414
5 Overview of displa y
Display Description Description
NET
GROSS
HOLD
BMI
Stability display Scales are in a steady state
Zeroing display
Net weight display Illuminated when net weight is displayed
Gross weight display Illuminat ed when gross weight is displayed
HOLD function HOLD function active
BMI function Illuminated while BMI function is enabled
Should the balance not display exactly
zero despite empty weighing plate, press
the button. Your balance will be set to
zero after a short standby time.
Illuminated after weighing scale was tared
MPC_M / MPE_HM / MPE_PM-BA-e-1414 13
Weighing instruments have to be verified for the purposes stated
Article 1,
mass in the practice of medicine
that is, weighing patients for reasons of medical supervision
during medical surveillance, examination and treatment.”
Indication
• Determining the body weight in the medical practice area.
steady display value is shown, you can read the weight value.
Contra-
• No contraindication known
Scales fitted with a serial interface may only be connected to
6 Basic Information (General)
below in accordance with Directive 2009/23/EC.
paragraph 4. “Determination of
6.1 Specific function
• Use as „non-standalone weighing scale“, that is, a person
steps carefully onto the weighing platform‘s centre. Once a
indication
6.2 Proper use
This weighing scale is designed for determining the weight of a person whilst
standing, such as in doctor’s surgeries. The balance is suitable for recognising,
preventing and controlling illnesses.
appliances in compliance with Directive EN60601-1.
On personal weighing scales, the person should step onto the centre of the weighing
platform and remain standing without moving.
As soon as a stable weighing value is reached the weighing value can be read.
The weighing scale is designed for continuous duty.
The weighing platform may only be stepped on by persons
capable of standing on both feet on the weighing platform.
The weighing platforms are fitted with an anti-slip surface that must not be covered
during weighing a person.
The balance should be checked for correct condition prior to each utilisation by a
person familiar with proper operation of the balance.
14 MPC_M / MPE_HM / MPE_PM-BA-e-1414
6.3 Improper Use
Do not use these scales for dynamic weighing processes.
Do not leave permanent load on the weighing pan. This may damage the measuring
system.
Impacts and overloading exceeding the stated maximum load (max) of the weighing
plate, minus a possibly existing tare load, must be strictly avoided. This could cause
damage to the balance.
Never operate balance in explosive environment. The serial version is not explosion
protected. It should be noted that a flammable mixture of anaesthetics and oxygen or
laughing gas may occur.
The structure of the balance may not be modified. This may lead to incorrect
weighing results, safety-related f ault s and des tr uct ion of the balance.
The balance may only be used according to the described conditions. Other areas of
use must be released by KERN in writing.
6.4 Warranty
Warranty claims shall be voided in case
• Our conditions in the operation manual are ignored
• The appliance is used outside the described uses
• The appliance is modified or opened
• Mechanical damage and damage caused by media, liquids,
• Natural wear and tear
• The appliance is improperly set up or incorrectly electrically connected
• The measuring system is overloaded
• Dropping the balance
6.5 Monitoring of Test Resources
In the framework of quality assurance the measuring-related weighing properties of
the balance and, if applicable, the testing weight, must be checked regularly. The
responsible user must define a suitable interval as well as type and scope of this test.
Information is available on KERN’s home page (www.kern-sohn.com with regard to
the monitoring of balance test substances and the test weights required for this. In
KERN’s accredited DKD calibration laboratory test weights and balances may be
calibrated (return to the national standard) fast and at moderate cost.
Using measuring technology to check the accuracy of the measuring device is
recommended for personal fl oor scal es with body height measurement but is not
absolutely essential as the calculation of the human body height is always subject to
a great deal of inaccuracy.
MPC_M / MPE_HM / MPE_PM-BA-e-1414 15
The original German is binding.
7 Basic Safety Precautions
7.1 Pay attention to the instructions in the Operation Manual
Car ef ull y read this operation manual bef ore
setup and commissioning, even if you are
already familiar with KERN balances.
All language versions contain a non-binding
7.2 Personnel training
The medical staff must apply and follow the operating instructions for proper use and
care of the product.
7.3 Preventing contamination
The prevention of cross-contamination (fungal skin infections …) requires regular
cleaning of the weighing platform. Recommendation: after a weighing procedure that
could potentially result in contamination (e. g. after weighing that involves direct skin
contact).
translation.
16 MPC_M / MPE_HM / MPE_PM-BA-e-1414
The installation and use of this electrical medical device requires
below.
Devices emitting high frequency signals (mobile telephones, radio
minimum distances.
8 Electromagnetic compat ibility (EMC)
8.1 General hints
special precautionary measures as outlined in the EMC information
This device complies with the limits set for medical electrical devices of group 1,
class B (as per EN 60601-1-2).
Electromagnetic compatibility (EMC) describes a device’s ability to perform reliably
within an electromagnetic environment without causing inadmissible electromagnetic
interference at the same time. Amo ng st other thi ng s , such disturbances may be
emitted by connecting cables or the air.
Inadmissible disturbances from the environment may result in incorrect displays,
inaccurate measured values or incorrect behaviour of the medical device. By the
same token the medical device may in some cases cause such disturbances in other
devices. To eliminate problems of that kind, we recommend you to take one or
several of the measures listed below:
• Change the alignment or distance of the device to the source of EMI.
• Install or use the floor scales MPC/MPE at a different location.
• Connect the floor scales MPC/MPE to a different power sour ce.
• For further questions please contact our customer services.
Disturbances may be caused by improper modification or add-ons to the device or
not recommended accessories (such as pow er units or con nect ing cables). The
manufacturer will not be responsible for these. Modifications may also result in a loss
of authorisation relating to the use of the device.
transmitters, radio receivers) may cause interference in the floor scale
MPC/MPE. For that reason do not use them near the fl oor scale
MPC/MPE. Chapter 8.4 contains details about recommended
MPC_M / MPE_HM / MPE_PM-BA-e-1414 17
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