Declaration of conformity – Precision Medical PM4130 EasyPulse POC3 User Manual

Page 19

Advertising
background image

18

Portable Oxygen Concentrator

DECLARATION OF CONFORMITY

Precision Medical, Inc.

300 Held Drive

Northampton PA 18067, USA

Emergo Europe (European Office)

Molenstraat 15

2513 BH, The Hague

The Netherlands

Phone: +31 (0) 70.345.8570

Fax: +31 (0) 70.346.7299

PM4130

Classification: IIa
Classification criteria: Clause 3.2 Rule 11 of Annex IX of MDD
We hereby declare that an examination of the under mentioned production quality

assurance system has been carried out following the requirements of the UK national

legislation to which the undersigned is subjected, transposing Annex II, 3 of the Directive

93/42/EEC and Directive 2007/47/EC on medical devices.

We certify that the production quality system conforms to the relevant provisions of the

aforementioned legislation, and the result entitles the organization to use the CE 0473

marking on those products listed above.
Applied Standards:

EN 1041, EN ISO 14971, EN 60601‑1, EN 60601‑1‑2, EN 60601‑1‑8,

EN 62366, EN ISO 3744, ISO 80601‑2‑67, ISO 80601‑2‑69,

EN ISO 15001, ISO 13485, ISO 15223‑1, 2006/66/EC,

2011/65/EC (RoHS 2)

Notified Body:

AMTAC Certification Services Limited

0473

Address:

Davy Avenue Knowlhill Milton Keynes MK5 8NL, UK

Certification Registration No’s: 1126 A CE

Date of Expiry: 26 July 2017

Devices already manufactured: S/N traceability Device History Records

Validity of DOC:

31 August 2012 to Date of Expiry

Manufacture Representative: Quality Manager
Position:

Quality Systems/ISO Representative

Date of Issue:

31 August 2012

Tell us how we are doing!

Visit us at www.precisionmedical.com

For technical specifications call Precision Medical or visit

wwwprecisionmedical.com

Advertising
This manual is related to the following products: