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 - PAUL MARIENFELD GMBH & CO KG

Address:

AM WOLLERSPFAD 4

LAUDA-KONIGSHOFEN

97922

Germany

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

Unit 80 Mochdre Enterprise Park

Newtown

Powys SY16 4LE

United Kingdom

Code/Term Type

Capillary blood collection tube IVD sodium heparin Capillary blood collection tube IVD sodium heparin IVD General

Microscope slide coverslip IVD Microscope slide coverslip IVD IVD General

Microscope counting chamber IVD Microscope counting chamber IVD IVD General

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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Code/Term		Type
Capillary blood collection tube IVD sodium heparin	Capillary blood collection tube IVD sodium heparin	IVD General
Microscope slide coverslip IVD	Microscope slide coverslip IVD	IVD General
Microscope counting chamber IVD	Microscope counting chamber IVD	IVD General
General specimen microscopy slide IVD single-use	General specimen microscopy slide IVD single-use	IVD General