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 - Sixtem Life S.r.l

Address:

Via Emilio Boni 19

Prato

Toscana 59100

Italy

Authorised Representative/ UK Responsible Person
Name: Diomed Developments Ltd
Address:

Tatmore Place Gosmore

Hitchin

Herts SG4 7QR

United Kingdom

Code/Term Type

Wart-removal cryogenic kit Wart-removal cryogenic kit Conformity Assessment Certificate Expired Class IIa

Wart-removal cryogenic kit Wart-removal cryogenic kit 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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Code/Term		Type
Wart-removal cryogenic kit	Wart-removal cryogenic kit Conformity Assessment Certificate Expired	Class IIa
Wart-removal cryogenic kit	Wart-removal cryogenic kit	Class IIa