Faaborg Rehab Technic Charder MS 6000 User Manual page 40

Manufacturer's Declaration of Conformity
This product has been manufactured in accordance with the
harmonized European standards, following the provisions of the
below stated directives:
Please see separate document showing on sticker of device for
above CE marking.
Authorized EU Representative:
Faaborg Rehab Technic ApS
Smedemestervej 9,
DK-5600 Faaborg
Denmark
Phono no.: +45 70 20 55 53/ E-mail: office@faaborg-rehab.dk
Manufactured by:
Charder Electronic Co., Ltd.
No.103, Guozhong Rd., Dali Dist.,
Taichung City 412, Taiwan (R.O.C.)
FDA no.: D072479
IN-1224 [12185H] 11/2016
93/42/EEC
2007/47/EC
Medical Device Directive
2014/31/EU
Non-automatic Weighing Instruments
Directive
- 39 -
as amended by