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CMS50M, Declaration of Conformity (CMS50M) PDF

This document is a Declaration of Conformity for a pulse oximeter (CMS50M) manufactured by CONTEC MEDICAL SYSTEMS CO., LTD to Council Directive 93/42/EEC concerning medical devices. The declaration states that the pulse oximeter meets the provisions of the directive including all amendments. Standards applied include IEC 60601-1, IEC 60601-1-2, IEC 60601-1-6, IEC 60601-1-11, IEC 62366, ISO 80601-2-61, and IEC 62304. TÜV SÜD Product Service GmbH is the notified body that issued the EC certificate.

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319 views2 pages

CMS50M, Declaration of Conformity (CMS50M) PDF

This document is a Declaration of Conformity for a pulse oximeter (CMS50M) manufactured by CONTEC MEDICAL SYSTEMS CO., LTD to Council Directive 93/42/EEC concerning medical devices. The declaration states that the pulse oximeter meets the provisions of the directive including all amendments. Standards applied include IEC 60601-1, IEC 60601-1-2, IEC 60601-1-6, IEC 60601-1-11, IEC 62366, ISO 80601-2-61, and IEC 62304. TÜV SÜD Product Service GmbH is the notified body that issued the EC certificate.

Uploaded by

parazitu38
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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DECLARATION OF CONFORMITY

TO COUNCIL DIRECTIVE 93/42/EEC


CONCERNING MEDICAL DEVICES
CONTEC MEDICAL SYSTEMS CO., LTD
No.112 Qinhuang West Street, Economic ＆Technical
MANUFACTURER: Development Zone, Qinhuangdao, Hebei Province,
PEOPLE’S REPUBLIC OF CHINA
MEDICAL DEVICE: Pulse Oximeter, CMS50M
CLASSIFICATION - ANNEX IX: Class Ⅱb, Rule 10
CONFORMITY ASSESSMENT ROUTE: Annex Ⅱexcluding chapter 4
WE, （CONTEC MEDICAL SYSTEMS CO., LTD） HEREWITH DECLARE THAT THE STATED
MEDICAL DEVICES. MEET THE TRANSPOSITION INTO NATIONAL LAW, THE PROVISIONS OF
COUNCIL DIRECTIVE 93/42/EEC OF 14 JUNE 1993 CONCERNING MEDICAL DEVICES;
INCLUDING, AT 21 MARCH 2010, THE AMENDMENTS BY COUNCIL DIRECTIVE 2007/47/EEC
ALL SUPPORTING DOCUMENTATION IS RETAINED AT THE PREMISES OF THE MANUFACTURE.

STANDARDS APPLIED: SEE ATTACHED LIST OF


(HARMONISED - EN) STANDARDS FOR WHICH
DOCUMENTED EVIDENCE OF COMPLIANCE CAN BE PROVIDED.

TÜV SÜD PRODUCT SERVICE GMBH


NOTIFIED BODY:
RIDLERSTR 65, D-80339 M NCHEN, GERMANY

IDENTIFICATION NUMBER:
0123

(EC) CERTIFICATE(S): G1 050972 0050 Rev.02

Shanghai International Holding Corp. GmbH(Europe)


EUROPEAN REPRESENTATIVE: Eiffestrasse 80, 20537 Hamburg Germany

START OF CE-MARKING: 2016-05-27 (Date or Lot or serial number)

PLACE, DATE OF DECLARATION: QINHUANGDAO,2019-07-23

President
SIGNATURE:

TF-CE100106-13 Ver:C

Page 1 of 2
DECLARATION OF CONFORMITY
TO COUNCIL DIRECTIVE 93/42/EEC
CONCERNING MEDICAL DEVICES
Appendix: list of (harmonised - EN) standards
NO. Reference Title
Medical electrical equipment - Part 1: General
1 IEC 60601-1:2012 requirements for basic safety and essential
performance
Medical electrical equipment- Part 1-2: General
requirements for basic safety and essential
2 IEC 60601-1-2:2007
performance - Collateral standard: Electromagnetic
compatibility
Medical electrical equipment-Part 1-6:General
3 IEC 60601-1-6:2010 requirements for basic safety and essential
performance-Collateral Standard: Usability
Medical electrical equipment -- Part 1-11: General
requirements for basic safety and essential
4 IEC 60601-1-11:2010 performance - Collateral standard: Requirements for
medical electrical equipment and medical electrical
systems used in the home healthcare environment
Medical devices - Application of usability engineering
5 IEC 62366:2007
to medical devices
Medical electrical equipment —Part 2-61: Particular
6 ISO 80601-2-61：2011 requirements for basic safety and essential
performance of pulse oximeter equipment

7 IEC 62304:2006 Medical device software-Software life-cycle processes

TF-CE100106-13 Ver:C

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