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 - BiopSafe ApS

Address:

Carolinevej 2A

Hellerup

2900

Denmark

Authorised Representative/ UK Responsible Person
Name: It's Interventional Regulatory Limited
Address:

Albreda House Lydgate Lane

Sheffield

South Yorkshire S10 5FH

England United Kingdom

Code/Term Type

General tissue specimen container IVD no additive General tissue specimen container IVD no additive 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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