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 188602. The device is manufactured by Cedarlane Corporation from Canada, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MedEnvoy 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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Complement reagent IVD

MHRA Device ID: 188602•Ref: 188602

Device Type

In Vitro Diagnostic Device

Devices

Complement reagent IVD

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Mar 12, 2024

Manufacturer Information

Name

Cedarlane Corporation

Address

4410 Paletta Court

Burlington, Canada

Created Date

Mar 7, 2024

Authorized Representative

Name

MedEnvoy UK Limited

Relationship Type

UK Responsible Person

Address

85 Great Portland Street First Floor

London, England, United Kingdom

Postcode: W1W 7LT

DJ Fang

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Other Products from Cedarlane Corporation (2)

Fluorescein-labelled aerolysin (FLAER) test IVD, reagent

Type: In Vitro Diagnostic Device

Registered: Nov 26, 2024

Complement reagent IVD

Type: In Vitro Diagnostic Device

Registered: Dec 14, 2021

Other Products from Same Authorized Representative (10)

Complement reagent IVD - UK MHRA Medical Device Registration

Device Type

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Date Registered

Last Updated

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Address

Created Date

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Relationship Type

Address

DJ Fang

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