EDAN INSTRUMENTS, INC
.
Manual Ver.: 1.3
Release Date: Nov. 2007
Part Number: MS1R-36708-V1.3
EC Declaration of Conformity
Manufacturer: EDAN Instruments, Inc.
Addr: 3/F-B, Nanshan Medical Equipments Park, Nanhai Rd 1019#, Shekou, Nanshan
Shenzhen, 518067 P.R. CHINA
European Representative:Shanghai International Holding Corp. GmbH (Europe)
Addr: Eiffestrasse 80 D-20537 Hamburg Germany
Product: Ultrasonic Pocket Doppler
Model: SONOTRAX Lite, SONOTRAX Basic, SONOTRAX Basic A, SONOTRAX Pro,
SONOTRAX II, SONOTRAX II Pro
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 M
Identification number
Ü
nchen, Germany.
I