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 - S.M.A.I.O

Address:

2 Place Berthe Morisot Parc Technologique

SAINT-PRIEST

69800

France

Authorised Representative/ UK Responsible Person
Name: Orthomotion Medical Ltd
Address:

Unit 1 Area A Creamery Industrial Estate Kenlis Road

Barnacre

Preston

Lancashire PR3 1GD

England United Kingdom

Code/Term Type

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

Internal spinal fixation procedure kit reusable Internal spinal fixation procedure kit reusable Class IIb

Internal spinal fixation procedure kit reusable Internal spinal fixation procedure kit 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
Bone-screw internal spinal fixation system non-sterile	Bone-screw internal spinal fixation system non-sterile	Class IIb
Internal spinal fixation procedure kit reusable	Internal spinal fixation procedure kit reusable	Class IIb
Internal spinal fixation procedure kit reusable	Internal spinal fixation procedure kit reusable	Class I