Urine specimen collection kit IVD - UK MHRA Medical Device Registration

Urine specimen collection kit IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 204625. The device is manufactured by DNA Genotek Inc. from Canada, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad UK Ltd..

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Urine specimen collection kit IVD

MHRA Device ID: 204625•Ref: 204625

Device Type

In Vitro Diagnostic Device

Devices

Urine specimen collection kit IVD

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Jun 26, 2024

Manufacturer Information

Name

DNA Genotek Inc.

Address

3000 - 500 Palladium Drive

Ottawa, Ontario, Canada

Created Date

Jun 7, 2024

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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Urine specimen collection kit IVD - UK MHRA Medical Device Registration

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Created Date

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DJ Fang

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