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 - pfm medical hico gmbh

Address:

Bonner Strausse 180

Koln

50968

Germany

Authorised Representative/ UK Responsible Person
Name: pfm medical UK Limited
Address:

Suite 3 Armcon Business Park London Road South

Poynton

Cheshire SK12 1LQ

England United Kingdom

Code/Term Type

Ultrasonic nebulizing system Ultrasonic nebulizing system Class IIa

Circulating-fluid whole-body heating/cooling system control unit Circulating-fluid whole-body heating/cooling system control unit Class IIb

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
Ultrasonic nebulizing system	Ultrasonic nebulizing system	Class IIa
Circulating-fluid whole-body heating/cooling system control unit	Circulating-fluid whole-body heating/cooling system control unit	Class IIb