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

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Manufacturer's Devices - pfm medical titanium gmbh

Address:

Sudwestpark 42

Nurnberg

90449

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

Hiatal hernia surgical mesh synthetic polymer non-bioabsorbable Hiatal hernia surgical mesh synthetic polymer non-bioabsorbable Class IIb

Extra-gynaecological surgical mesh synthetic polymer non-bioabsorbable Extra-gynaecological surgical mesh synthetic polymer non-bioabsorbable Class IIb

Multi-purpose surgical mesh synthetic polymer non-bioabsorbable non-antimicrobial Multi-purpose surgical mesh synthetic polymer non-bioabsorbable non-antimicrobial Class IIb

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
Hiatal hernia surgical mesh synthetic polymer non-bioabsorbable	Hiatal hernia surgical mesh synthetic polymer non-bioabsorbable	Class IIb
Extra-gynaecological surgical mesh synthetic polymer non-bioabsorbable	Extra-gynaecological surgical mesh synthetic polymer non-bioabsorbable	Class IIb
Multi-purpose surgical mesh synthetic polymer non-bioabsorbable non-antimicrobial	Multi-purpose surgical mesh synthetic polymer non-bioabsorbable non-antimicrobial	Class IIb