Public Access Database for Medical Device Registration

Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA)
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity

Manufacturer's By Name

By Device

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Manufacturer's Devices - Coral Clinical Systems - A Division of Tulip Diagnostics (P) Ltd.

Address:

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

Verna

Goa 403722

India

Authorised Representative/ UK Responsible Person
Name: CMC Medical Devices LTD
Address:

Office 32 19-21 Crawford Street

London

W1H 1PJ

United Kingdom

Code/Term Type

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

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

Urea IVD reagent Urea IVD reagent IVD General

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

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Code/Term		Type
Creatine kinase myocardial isoenzyme (CKMB) IVD kit enzyme spectrophotometry	Creatine kinase myocardial isoenzyme (CKMB) IVD kit enzyme spectrophotometry	IVD General
Total creatine kinase (CK) IVD kit enzyme spectrophotometry	Total creatine kinase (CK) IVD kit enzyme spectrophotometry	IVD General
Urea IVD reagent	Urea IVD reagent	IVD General