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

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Manufacturer's Devices - pfm medical AG

Address:

Wankelstrasse 60

Cologne

50996

Germany

Authorised Representative/ UK Responsible Person
Name: pfm medical UK Limited
Address:

Suite 3 Armcon Business Park London Road South

Poynton

Cheshire SK12 1LQ

England United Kingdom

Code/Term Type

Rotary microtome IVD Rotary microtome IVD IVD General

Sliding microtome IVD Sliding microtome IVD 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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Code/Term		Type
Rotary microtome IVD	Rotary microtome IVD	IVD General
Sliding microtome IVD	Sliding microtome IVD	IVD General