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 - SKANLAB AS

Address:

Stadion 29 3e etg

Krakeroy

NO-1671

Norway

Authorised Representative/ UK Responsible Person
Name: PHOENIX HEALTHCARE PRODUCTS LTD
Address:

Unit 15 Calverton Business Park HOYLE ROAD

CALVERTON NOTTINGHAM

CALVERTON NOTTINGHAM

NOTTINGHAM NG14 6QL

England United Kingdom

Code/Term Type

Medium-wave diathermy treatment system Medium-wave diathermy treatment system 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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