General specimen container IVD, additive/medium - UK MHRA Medical Device Registration

General specimen container IVD, additive/medium is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 110225. The device is manufactured by Asuragen, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Emergo Consulting (UK) Limited .

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General specimen container IVD, additive/medium

MHRA Device ID: 110225•Ref: 110225

Device Type

In Vitro Diagnostic Device

Devices

General specimen container IVD, additive/medium

Type

IVD General

Date Registered

Jul 8, 2024

Last Updated

Apr 17, 2024

Manufacturer Information

Name

Asuragen, Inc.

Address

2150 Woodward Street Suite 100

Austin, Texas, United States

Created Date

Oct 28, 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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General specimen container IVD, additive/medium - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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Created Date

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DJ Fang

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