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CE Marking
  Authorized Representative for  
  SentioLife Solutions Ltd
 
Medical Devices

 (Service renewal needed by: 27 January 2014 ) 

| Products | CE Marking | Authorized Representative | Manufacturer | Importer/Distributor |


Products



Please learn more about the products at


CE Marking

Represented by Wellkang since:27 February 2012
Wellkang Auth Rep Certificates no.:ARMDD121059B130410LN (Valid until: 26 February 2014)
ARMDD121059A120319LN (Valid until: 26 February 2013)
Notified Body:NOT applicable
(for class I MD non-sterile, without measuring function)
Product Classification:Class I Medical Devices, non-sterile, without measuring function
(under MDD Directive 93/42/eec)
Conformity Modules: Module A
EC Declaration of Conformity (Annex VII) + Technical File
Lead Competent Authority:UK Medicines & Healthcare Products Regulatory Agency
Product Registration Ref. No.:
(Per Article 14, Directive 93/42/eec.)
CA013154
Click here to view the registration certificate.



Authorized Representative
in the European Economic Area (incl. European Union and EFTA member states):

Wellkang Ltd
Suite B, 29 Harley Street
LONDON W1G 9QR, United Kingdom
Tels: +44(20)30869438/32876300     Fax: +44(20)76811874
Web: www.CE-marking.eu   www.CE-marking.com    www.wellkang.com



Manufacturer

SentioLife Solutions Ltd
CP210, 1076 hwy 335, Middle West Pubnico,
Nova Scotia, B0W 2M0,
Canada
Phs: +1-902-7620186 or 7480851
F: +1-902-7620420
W: www.sentiolifesolutions.com
Email: (available but not published here)



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Last updated on 10/April/2013