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 171205. The device is manufactured by Novosanis NV from Belgium, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Emergo Consulting (UK) 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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In Vitro Diagnostic Device

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General specimen container IVD, additive/medium

MHRA Device ID: 171205•Ref: 171205

Device Type

In Vitro Diagnostic Device

Devices

General specimen container IVD, additive/medium

Type

Class A

Date Registered

Nov 26, 2024

Last Updated

Apr 17, 2024

Manufacturer Information

Name

Novosanis NV

Address

Bijkhoevelaan 32c

Wijnegem, Belgium

Created Date

Feb 2, 2022

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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Other Products from Novosanis NV (2)

General specimen container IVD, no additive/medium

Type: In Vitro Diagnostic Device

Registered: Nov 26, 2024

General specimen container IVD, no additive/medium

Type: In Vitro Diagnostic Device

Registered: Nov 26, 2024

Other Products from Same Authorized Representative (10)

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

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