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 - Qlicksmart Pty Ltd

Address:

148 Boundary Street Level 1

West End

Brisbane

Queensland 4101

Australia

Authorised Representative/ UK Responsible Person
Name: THE KOPPERS CARE LIMITED
Address:

The Street

Kilmington

Devon EX13 7RJ

England United Kingdom

Code/Term Type

Scalpel blade remover Scalpel blade remover Class I

Scalpel blade remover sterile Scalpel blade remover sterile Class I

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
Scalpel blade remover	Scalpel blade remover	Class I
Scalpel blade remover sterile	Scalpel blade remover sterile	Class I