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 - Zimmer MedizinSysteme GmbH

Address:

Junkersstraße 9 Neu-Ulm

Neu-Ulm

89231

Germany

Authorised Representative/ UK Responsible Person
Name: NewMed Ltd
Address:

Station Yard Station Road

Harrietsham Maidstone

Maidstone

Kent ME17 1JA

England United Kingdom

Code/Term Type

Electromechanical orthopaedic extracorporeal shock wave therapy system Electromechanical orthopaedic extracorporeal shock wave therapy system Class IIa

Localized cutaneous/musculoskeletal cryotherapy unit Localized cutaneous/musculoskeletal cryotherapy unit Class IIa

Deep-tissue electromagnetic stimulation system professional Deep-tissue electromagnetic stimulation system professional Class IIa

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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Code/Term		Type
Electromechanical orthopaedic extracorporeal shock wave therapy system	Electromechanical orthopaedic extracorporeal shock wave therapy system	Class IIa
Localized cutaneous/musculoskeletal cryotherapy unit	Localized cutaneous/musculoskeletal cryotherapy unit	Class IIa
Deep-tissue electromagnetic stimulation system professional	Deep-tissue electromagnetic stimulation system professional	Class IIa
Medium-wave diathermy treatment system	Medium-wave diathermy treatment system	Class IIa