Charder HM200P Скачать руководство пользователя страница 2

2

 

Explanation of Text/Symbols on Device Label/Packaging 

 

Text/Symbol 

Meaning 

 

Caution, consult accompanying documents before use 

 

Separate  collection  for  waste  of  electrical  and  electronic  equipment,  in 

accordance  with  Directive  2002/96/EC.  Do  not  dispose  of  device  with 
everyday waste 

 

Name and address of device manufacturer, and year/country of manufacture 

 

Carefully  read  user  manual  before  installation  and  usage,  and  follow 
instructions for use. 

 

Device catalogue number / model number 

 

Name and address of authorized representative in the European Union 

 

Device is a medical device. Text indicates device category type 

 

Manufacturer's batch or lot number for device 

 

Device's serial number 

 

Device's Unique Device Identifier 

 

Device conforms to 93/42/EEC as amended by 2007/47/EC Medical Device 
Directive. Four digit number is identifier for medical device Notified Body 

 

Name and address of entity importing device (if applicable) 

 

Name and address of entity responsible for translating Information For 

Use (if applicable) 

 

Copyright Notice 

Charder Electronic Co., Ltd.   

No.103, Guozhong Rd., Dali Dist., Taichung City 41262 Taiwan 

Tel: +886-4-2406 3766  

Fax: +886-4-2406 5612 

Website: www.chardermedical.com  

E-mail: [email protected] 

 
Copyright©  Charder Electronic Co., Ltd. All rights reserved. 

This user manual is protected by international copyright law. All content is licensed, and usage 

is subject to written authorization from Charder Electronic Co., Ltd. (hereinafter Charder) 

Charder is not liable for any damage caused by a failure to adhere to requirements stated in 

this manual. Charder reserves the right to correct misprints in the manual without prior notice, 

and modify the exterior of the device for quality purposes without customer consent. 

 

 

Charder Electronic Co., Ltd. 

No. 103, Guozhong Rd., Dali Dist., 

Taichung City, 41262 Taiwan

Содержание HM200P

Страница 1: ...1 USER MANUAL HM200P Portable Height Stadiometer Please keep the instruction manual at hand all the time for future reference...

Страница 2: ...git number is identifier for medical device Notified Body Name and address of entity importing device if applicable Name and address of entity responsible for translating Information For Use if applic...

Страница 3: ...3 CONTENTS I Safety Notes 4 A General Information 4 II Installation 6 Unpacking the HM200P 6 Assembly Instructions 7 III Using Device 9 IV Product Specifications 10 V Declaration of Conformity 12...

Страница 4: ...designed to be used in accordance with national regulations to measure height within specifications for height related usage by professionals Clinical Benefit Measurement results can be used by profe...

Страница 5: ...wing reasons unsuitable or improper storage or use incorrect installation or commissioning by the owner or third parties natural wear and tear changes or modifications incorrect or negligent handling...

Страница 6: ...6 II Installation Unpacking the HM200P Head stopper Height Rod 4 Base platform Support plate...

Страница 7: ...7 Assembly Instructions 1 Remove support plate 2 Insert Height Rods into base platform in order 3 Ensure that height rods are inserted in the correct order 4 Mount head stopper onto height rod...

Страница 8: ...8 5 Place support plate on top of height rod 6 Place HM200P against the wall for stability...

Страница 9: ...ect should stand up straight with feet within the foot markings 2 Subject s back should tough the height measurement rod slightly Lower stopper until it touches top of subject s head 3 Read height mea...

Страница 10: ...5 81 in Graduation 1 mm 1 16 in Accuracy 10 mm Dimensions Overall 350 W x 400 D x 2430 H mm Device Weight approximate 2 0 kg 4 4 lb carry case 0 6 kg 1 3 lb Operation Temperature Humidity 5 35 Optiona...

Страница 11: ...____________________ _______________________________________________________ _______________________________________________________ _______________________________________________________ ___________...

Страница 12: ...ollowing directives 93 42 EEC as amended by 2007 47 EC Medical Device Directive Classification Class I with measuring function RoHS Directive 2011 65 EU and Delegated Directive EU 2015 863 Authorized...

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