Adenovirus antigen IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Adenovirus antigen IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 173791. The device is manufactured by TIB Molbiol Syntheselabor Gmbh from Germany, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Roche Diagnostics Limited.

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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Adenovirus antigen IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 173791•Ref: 173791

Device Type

In Vitro Diagnostic Device

Devices

Adenovirus antigen IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Nov 15, 2024

Manufacturer Information

Name

TIB Molbiol Syntheselabor Gmbh

Address

Eresburgstraße 22–23

Berlin, Germany

Created Date

Feb 9, 2022

Authorized Representative

Name

Roche Diagnostics Limited

Relationship Type

UK Responsible Person

Address

Roche Diagnostics Limited Charles Avenue

Burgess Hill, West Sussex, United Kingdom

Postcode: RH15 9RY

DJ Fang

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Adenovirus antigen IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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