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 - NOVAGENIT SRL

Address:

Viale Trento 115/117

MEZZOLOMBARDO

TRENTO (TN) 38017

Italy

Authorised Representative/ UK Responsible Person
Name: ADLER ORTHO UK LTD
Address:

Castle Chambers 43 Castle Street

Liverpool

L2 9TL

England United Kingdom

Code/Term Type

Tendon/ligament bone anchor bioabsorbable Tendon/ligament bone anchor bioabsorbable Class III

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

General laboratory container single-use sterile General laboratory container single-use sterile Class I

Implantable-device infection control barrier Implantable-device infection control barrier Class III

Subtalar implant bioabsorbable Subtalar implant bioabsorbable Class I

Bone matrix implant composite Bone matrix implant composite Class I

Surgical anti-adhesion material implantable bioabsorbable non-medicated Surgical anti-adhesion material implantable bioabsorbable non-medicated Class III

Cartilage biomatrix implant animal-derived Cartilage biomatrix implant animal-derived Class III

Osteochondral matrix implant Osteochondral matrix implant Class III

Osteochondral matrix implant Osteochondral matrix implant Class III

Osteochondral matrix implant Osteochondral matrix implant Class III

Osteochondral matrix implant Osteochondral matrix implant Class III

Osteochondral matrix implant Osteochondral matrix implant Class III

Osteochondral matrix implant Osteochondral matrix implant Class III

Osteochondral matrix implant Osteochondral matrix implant Class III

Osteochondral matrix implant Osteochondral matrix implant Class III

Osteochondral matrix implant Osteochondral matrix implant Class III

Osteochondral matrix implant Osteochondral matrix implant Class III

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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