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Complement reagent IVD - UK MHRA Medical Device Registration

Complement reagent IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 121110. The device is manufactured by Cedarlane Corporation from Canada, classified as In Vitro Diagnostic Device. The authorized representative in the UK is V. H. Bio 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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Complement reagent IVD
MHRA Device ID: 121110โ€ขRef: 121110

Device Type

In Vitro Diagnostic Device

Devices

Complement reagent IVD

Type

IVD General

Date Registered

Dec 14, 2021

Last Updated

Dec 14, 2022

Manufacturer Information

Address

4100 Paletta Court

Burlington, Ontario, Canada

Created Date

Dec 14, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Unit 11B Station Approach Team Valley Trading Estate

Gateshead, England, United Kingdom

Postcode: NE11 0ZF

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