Urea IVD, reagent - UK MHRA Medical Device Registration

Urea IVD, reagent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 142500. The device is manufactured by Coral Clinical Systems - A Division of Tulip Diagnostics (P) Ltd. from India, classified as In Vitro Diagnostic Device. The authorized representative in the UK is CMC Medical Devices LTD.

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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Urea IVD, reagent

MHRA Device ID: 142500•Ref: 142500

Device Type

In Vitro Diagnostic Device

Devices

Urea IVD, reagent

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 4, 2023

Manufacturer Information

Name

Coral Clinical Systems - A Division of Tulip Diagnostics (P) Ltd.

Address

Bldg. D, Plot No. M-46, Phase IIIB, Verna Industrial Estate,

Verna, Goa, India

Created Date

Mar 30, 2022

Authorized Representative

Name

CMC Medical Devices LTD

Relationship Type

UK Responsible Person

Address

Office 32 19-21 Crawford Street

London, United Kingdom

Postcode: W1H 1PJ

DJ Fang

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Other Products from Coral Clinical Systems - A Division of Tulip Diagnostics (P) Ltd. (2)

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Type: In Vitro Diagnostic Device

Registered: Nov 26, 2024

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Type: In Vitro Diagnostic Device

Registered: Nov 26, 2024

Other Products from Same Authorized Representative (10)

Urea IVD, reagent - UK MHRA Medical Device Registration

Device Type

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Date Registered

Last Updated

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Address

Created Date

Name

Relationship Type

Address

DJ Fang

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Creatine kinase myocardial isoenzyme (CKMB) IVD, kit, enzyme spectrophotometry

Total creatine kinase (CK) IVD, kit, enzyme spectrophotometry

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