Blood lancet, single-use - UK MHRA Medical Device Registration

Blood lancet, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 96596. The device is manufactured by HTL-Strefa S.A. from Poland, classified as General Medical Device. The authorized representative in the UK is Qserve Group UK, Ltd. .

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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Blood lancet, single-use

MHRA Device ID: 96596•Ref: 96596

Device Type

General Medical Device

Devices

Blood lancet, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

HTL-Strefa S.A.

Address

ul. Adamówek 7

Ozorków, Poland

Created Date

Aug 20, 2021

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

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Other Products from HTL-Strefa S.A. (2)

Autoinjector needle

Type: General Medical Device

Registered: Nov 26, 2024

Manual blood lancing device, reusable

Type: General Medical Device

Registered: Nov 26, 2024

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Blood lancet, single-use - UK MHRA Medical Device Registration

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