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 - AngioSystems Inc

Address:

7 Hopkins Place

Ducktown

Tennessee 37326

United States

Authorised Representative/ UK Responsible Person
Name: Qserve Group UK Ltd.
Address:

49 Greek Street

London

W1D 4EG

England United Kingdom

Code/Term Type

Patient surgical drape single-use Patient surgical drape single-use Class I

Patient radiation shielding pad/drape single-use Patient radiation shielding pad/drape single-use Class I

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
Patient surgical drape single-use	Patient surgical drape single-use	Class I
Patient radiation shielding pad/drape single-use	Patient radiation shielding pad/drape single-use	Class I