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 - HTL-Strefa S.A.

Address:

ul. Adamówek 7

Ozorków

95-035

Poland

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

49 Greek Street

London

W1D 4EG

England United Kingdom

Code/Term Type

Manual blood lancing device reusable Manual blood lancing device reusable Class IIa

Autoinjector needle Autoinjector needle Class IIa

Blood lancet single-use Blood lancet single-use 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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Code/Term		Type
Manual blood lancing device reusable	Manual blood lancing device reusable	Class IIa
Autoinjector needle	Autoinjector needle	Class IIa
Blood lancet single-use	Blood lancet single-use	Class IIa