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 - X-os S.A.

Address:

Via Nassa 60

Lugano

6900

Switzerland

Authorised Representative/ UK Responsible Person
Name: International Limb Lengthening Clinic Ltd
Address:

38 Craven Street

London

WC2N 5NG

England United Kingdom

Code/Term Type

Diaphysis prosthesis Diaphysis prosthesis Class IIb

Orthopaedic bone screw non-bioabsorbable sterile Orthopaedic bone screw non-bioabsorbable sterile Class IIb

Cannulated surgical drill bit reusable Cannulated surgical drill bit reusable Class IIb

General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit Class IIa

General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit 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
Diaphysis prosthesis	Diaphysis prosthesis	Class IIb
Orthopaedic bone screw non-bioabsorbable sterile	Orthopaedic bone screw non-bioabsorbable sterile	Class IIb
Cannulated surgical drill bit reusable	Cannulated surgical drill bit reusable	Class IIb
General internal orthopaedic fixation system implantation kit	General internal orthopaedic fixation system implantation kit	Class IIa
General internal orthopaedic fixation system implantation kit	General internal orthopaedic fixation system implantation kit	Class I