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 - Ames Medical Prosthetic Soulutions SAU

Address:

Polígono Industrial Les Fallulles Ctra. Laureà Miró 388

Sant Feliu de Llobregat

08980

Spain

Authorised Representative/ UK Responsible Person
Name: Templar Regulatory Consulting Limited
Address:

Niall House Unit 4 24-26 Boulton Road

Stevenage

Stevenage

Hertfordshire SG14QX

England United Kingdom

Code/Term Type

Metallic osteotomy fusion cage non-customized Metallic osteotomy fusion cage non-customized Class IIb

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

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
Metallic osteotomy fusion cage non-customized	Metallic osteotomy fusion cage non-customized	Class IIb
Orthopaedic surgical procedure kit non-medicated single-use	Orthopaedic surgical procedure kit non-medicated single-use	Class IIa