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 - AREX

Address:

3 allee du Clos Tonnerre

Palaiseau

91125

France

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

External orthopaedic fixation system single-use sterile External orthopaedic fixation system single-use sterile Class IIb

Tendon spacer Tendon spacer 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
External orthopaedic fixation system single-use sterile	External orthopaedic fixation system single-use sterile	Class IIb
Tendon spacer	Tendon spacer	Class IIb