Multiple gastrointestinal virus nucleic acid IVD, reagent - UK MHRA Medical Device Registration

Multiple gastrointestinal virus nucleic acid IVD, reagent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 135841. 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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Multiple gastrointestinal virus nucleic acid IVD, reagent

MHRA Device ID: 135841•Ref: 135841

Device Type

In Vitro Diagnostic Device

Devices

Multiple gastrointestinal virus nucleic acid IVD, reagent

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

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Multiple gastrointestinal virus nucleic acid IVD, reagent - UK MHRA Medical Device Registration

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Created Date

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DJ Fang

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