Draegerwerk and KGaA EASTM21 Inductive Tag Reader module User Manual title

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Document ID	900906
Application ID	DM6uXbOXkBl4UBReviOn+g==
Document Description	Users Manual
Short Term Confidential	No
Permanent Confidential	No
Supercede	No
Document Type	User Manual
Display Format	Adobe Acrobat PDF - pdf
Filesize	1.83kB (22845 bits)
Date Submitted	2008-02-12 00:00:00
Date Available	2008-03-28 00:00:00
Creation Date	2007-10-29 17:58:25
Producing Software	Acrobat Distiller 6.0.1 (Windows)
Document Lastmod	2007-10-29 17:58:48
Document Title	title
Document Creator	Acrobat PDFMaker 6.0 for Word
Document Author:	Drgerwerk AG

Project file Module M21: 10.1 Instruction for use (IFU)
title
10.1 Instruction for use (IFU)
responsible
creating system
Gerd Wotha
MS-Word
author
document type
Gerd Wotha
doc
filling
KM-tool
Design history file
tbd
filling name and path
I:\Techn Management\Projekte\Electronic_Accessory_Signature_System\DPProject\05-Qualification\CE & FCC Akte\CE-Akte\10 Device Labelling\10.1 IfU incl accessory
list\10.1 Instruction for use (IFU).doc
Released
name
date
signature
Gerd Wotha
1. Instruction for use of Medical device
1.1. Declaration of conformity
A declaration of conformity according to R&TTE will be inserted to each instruction for use
of the Medical device which uses the Module M21.
1.2. General items
M21 Reader Module is an integrated part within Draeger Medical devices. The
antennas are permanently connected to the M21 via connectors.
M21 Reader Module has an operational manual. The programming of the Draeger
Medical device is based on this document. There is no user interface to the module.
1.3. Mandatory text
Changes or modifications not expressly approved by the party responsible for compliance
could void the user’s authority to operate the equipment
The intended use of the M21 will be explained within each instruction for use of the
Medical device which uses the Module M21.
Following text has to be content of the device IFU:
This device complies with Part 15 of the FCC Rules. Operation is subject to the following
two conditions: (1) this device may not cause harmful interference, and (2) this device
must accept any interference received, including interference that may cause undesired
operation.
revision
03
revision date
release status
Page 1 of 1
16.07.2007
released if signed
T:\Projekte\TCB USA\Draeger Medical AG & Co. KG\UVFEAST-MP02001\10.1 Instruction for use (IFU)-Rev3.doc

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