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 - Hammarplast Medical AB

Address:

Kartåsgatan 8

Lidköping

531 40

Sweden

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

Pure Offices Plato Close

Warwick

CV34 6WE

England United Kingdom

Code/Term Type

Medicine cup single-use Medicine cup single-use Class I

Tourniquet cuff single-use Tourniquet cuff single-use Class I

Ear speculum single-use Ear speculum single-use Class I

Tourniquet cuff reusable Tourniquet cuff reusable Class I

Tourniquet cuff reusable Tourniquet cuff reusable 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
Medicine cup single-use	Medicine cup single-use	Class I
Tourniquet cuff single-use	Tourniquet cuff single-use	Class I
Ear speculum single-use	Ear speculum single-use	Class I
Tourniquet cuff reusable	Tourniquet cuff reusable	Class I
Tourniquet cuff reusable	Tourniquet cuff reusable	Class I