10 APPENDIX A, EC DECLARATION OF CONFORMITY

EC Declaration of Conformity

Manufactured for

GF Health Products, Inc., 2935 Northeast Parkway,

 

Atlanta, GA 30360

 

 

Product

Ultrasound Pocket Doppler

 

 

Classification

(MDD, Annex IX): IIa

We herewith declare that the above mentioned product(s) meet the transposition into national law, the provisions of Council Directive 93/42/EEC of 14 June 1993 concerning medical devices - as amended by Directive 98/79/EC on in vitro diagnostic medical devices.

All supporting documentation is retained at the premises of the manufacturer.

Directives

General Applicable Directives: Medical Device

 

Directive: COUNCIL DIRECTIVE 93/42/EEC of 14

 

June 1993 concerning medical devices (MDD 93/42/

 

EEC).

Standards applied

EN ISO 9001, ISO13485, EN ISO14971, EN ISO10993-

 

1, IEC 601-1, EN 60601-1-1, BS EN 60601-1-4, IEC

 

60601-1-2, EN 61157, EN 1041, EN 60417-2-2000,

 

IEC/TR 60878-2003, EN 980, EN 55011, ISO 1000, YY

 

0111-93, EN 61266, EN ISO 780 , GB/T 14740, GB/T

 

15464

Notified Body

TÜV SÜD Product Service GmbH, Ridlerstr 65, D-

 

80339 MÜnchen, Germany.

Identification

 

number

 

 

 

14423-INS-LAB-RevD11

35

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Graham Field 14423-4, 14423-2, 14423-8 user manual Appendix A, EC Declaration of Conformity