Clinical specimen extraction buffer IVD - UK MHRA Medical Device Registration

Clinical specimen extraction buffer IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 189347. The device is manufactured by SENTINEL CH. S.p.A. from Italy, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad UK Ltd..

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Clinical specimen extraction buffer IVD

MHRA Device ID: 189347•Ref: 189347

Device Type

In Vitro Diagnostic Device

Devices

Clinical specimen extraction buffer IVD

Type

Class A

Date Registered

Nov 26, 2024

Last Updated

Oct 17, 2024

Manufacturer Information

Name

SENTINEL CH. S.p.A.

Address

Via Robert Koch 2 Milano

MI, Lombardia, Italy

Created Date

Aug 4, 2021

Authorized Representative

Name

Qarad UK Ltd.

Relationship Type

UK Responsible Person

Address

8 Northumberland Ave

Westminster, London , England, United Kingdom

Postcode: WC2N 5BY

DJ Fang

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Clinical specimen extraction buffer IVD - UK MHRA Medical Device Registration

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