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 - ENRAF-NONIUS B.V.

Address:

Vareseweg 127

Rotterdam

Z-H 3047AT

Netherlands

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

Physical therapy ultrasound/neuromuscular stimulation system Physical therapy ultrasound/neuromuscular stimulation system Class IIa

Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation 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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Code/Term		Type
Physical therapy ultrasound/neuromuscular stimulation system	Physical therapy ultrasound/neuromuscular stimulation system	Class IIa
Physical therapy transcutaneous neuromuscular electrical stimulation system	Physical therapy transcutaneous neuromuscular electrical stimulation system	Class IIa