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 - Cardia Innovation AB

Address:

Manskarsvagen 10B

Kungens Kurva

141 75 Kungens Kurva

Sweden

Authorised Representative/ UK Responsible Person
Name: Chalice Medical Ltd
Address:

Manton Wood Enterprise Park

Worksop

Nottinghamshire S80 2RS

United Kingdom

Code/Term Type

Surgical wound gas diffuser Surgical wound gas diffuser Class IIa

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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