Oral/respiratory tract specimen container IVD, additive/medium - UK MHRA Medical Device Registration

Oral/respiratory tract specimen container IVD, additive/medium is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 164337. The device is manufactured by DNA Genotek Inc. from Canada, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Emergo Consulting (UK) Limited .

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In Vitro Diagnostic Device

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Oral/respiratory tract specimen container IVD, additive/medium

MHRA Device ID: 164337•Ref: 164337

Device Type

In Vitro Diagnostic Device

Devices

Oral/respiratory tract specimen container IVD, additive/medium

Type

Class A

Date Registered

Jun 24, 2024

Last Updated

Apr 17, 2024

Manufacturer Information

Name

DNA Genotek Inc.

Address

3000 - 500 Palladium Drive

Ottawa, Ontario, Canada

Created Date

Nov 23, 2021

Authorized Representative

Name

Emergo Consulting (UK) Limited

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 – UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

DJ Fang

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Oral/respiratory tract specimen container IVD, additive/medium - UK MHRA Medical Device Registration

Device Type

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Date Registered

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Created Date

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Address

DJ Fang

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