Public Access Database for Medical Device Registration

Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA)
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity

Manufacturer's By Name

By Device

Back to MHRA

Manufacturer's Devices - Waldemar Knittel Glasbearbeitungs GmbH

Address:

Varrentrappstrasse 5

Braunschwqeig

38114

Germany

Authorised Representative/ UK Responsible Person
Name: CellPath Ltd
Address:

Unit 80 Mochdre Enterprise Park

Newtown

Powys SY16 4LE

United Kingdom

Code/Term Type

General specimen microscopy slide IVD single-use General specimen microscopy slide IVD single-use IVD General

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

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