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 - Caltag Medsystems Ltd

Address:

Whiteleaf Business Centre 11 Little Balmer

Buckingham

MK18 1TF

England United Kingdom

Authorised Representative/ UK Responsible Person
Name: Not Available

Address:

Code/Term Type

Evacuated blood collection tube IVD anticoagulant/cell preservative Evacuated blood collection tube IVD anticoagulant/cell preservative IVD General

General specimen container IVD additive/medium General specimen container IVD additive/medium Class A

Cell preservation/storage/dilution solution IVD Cell preservation/storage/dilution solution IVD Class A

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
Evacuated blood collection tube IVD anticoagulant/cell preservative	Evacuated blood collection tube IVD anticoagulant/cell preservative	IVD General
General specimen container IVD additive/medium	General specimen container IVD additive/medium	Class A
Cell preservation/storage/dilution solution IVD	Cell preservation/storage/dilution solution IVD	Class A