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 - PluroGen Therapeutics LLC

Address:

2495 General Armistead Avenue Suite B

Norristown

PA PA 19403

United States

Authorised Representative/ UK Responsible Person
Name: Medline Industries Ltd
Address:

3rd Floor Quayside Wilderspool Business Park Greenalls Avenue

Warrington

WA4 6HL

England United Kingdom

Code/Term Type

Wound hydrogel dressing non-antimicrobial Wound hydrogel dressing non-antimicrobial Class IIa

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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