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 - MPS Micro Precision Systems AG

Address:

Chemin du Long-Champ 95

Biel-Bienne

2504

Switzerland

Authorised Representative/ UK Responsible Person
Name: Emergo Consulting (UK) Limited
Address:

Compass House Vision Park Histon c/o Cr360 – UL International

Cambridge

CB24 9BZ

England United Kingdom

Code/Term Type

Orthopaedic implant driver Orthopaedic implant driver Class I

Surgical screwdriver reusable Surgical screwdriver reusable Class I

Surgical drill guide reusable Surgical drill guide reusable Class I

Bone nail guidewire reusable Bone nail guidewire reusable Class I

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
Orthopaedic implant driver	Orthopaedic implant driver	Class I
Surgical screwdriver reusable	Surgical screwdriver reusable	Class I
Surgical drill guide reusable	Surgical drill guide reusable	Class I
Bone nail guidewire reusable	Bone nail guidewire reusable	Class I