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

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Manufacturer's Devices - Safe Orthopaedics SAS

Address:

PARC DES BELLEVUES Allée Rosa Luxemburg

Batiment Le californie

ERAGNY SUR OISE

95610

France

Authorised Representative/ UK Responsible Person
Name: SAFE ORTHOPAEDICS Ltd
Address:

23 Copenhagen Street

London

N1 0JB

England United Kingdom

Code/Term Type

Orthopaedic surgical procedure kit non-medicated single-use Orthopaedic surgical procedure kit non-medicated single-use Class IIa

Bone-screw internal spinal fixation system sterile Bone-screw internal spinal fixation system sterile Class IIb

Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage 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
Orthopaedic surgical procedure kit non-medicated single-use	Orthopaedic surgical procedure kit non-medicated single-use	Class IIa
Bone-screw internal spinal fixation system sterile	Bone-screw internal spinal fixation system sterile	Class IIb
Polymeric spinal interbody fusion cage	Polymeric spinal interbody fusion cage	Class IIb