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 - EUROSPINE SARL

Address:

3 Avenue des Dahlias

L'Haÿ-les-Roses

94240

France

Authorised Representative/ UK Responsible Person
Name: QARA Business Solutions Ltd
Address:

Coverdale House 10 Purshall Close

Redditch

Redditch

Worcestershire B974PD

United Kingdom

Code/Term Type

Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Class IIb

Spinal implant trial Spinal implant trial Class IIa

Orthopaedic prosthesis implantation positioning instrument reusable Orthopaedic prosthesis implantation positioning instrument reusable Class I

Device sterilization/disinfection container reusable Device sterilization/disinfection container 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
Polymeric spinal interbody fusion cage	Polymeric spinal interbody fusion cage	Class IIb
Spinal implant trial	Spinal implant trial	Class IIa
Orthopaedic prosthesis implantation positioning instrument reusable	Orthopaedic prosthesis implantation positioning instrument reusable	Class I
Device sterilization/disinfection container reusable	Device sterilization/disinfection container reusable	Class I