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 - Active Implants Israel Ltd.

Address:

43 Hamelacha Street Sapir Industrial Park South

Natanya

42505

Israel

Authorised Representative/ UK Responsible Person
Name: Emergo Consulting (UK) Limited
Address:

Compass House Vision Park Histon c/o Cr360 – UL International

Cambridge

CB24 9BZ

England United Kingdom

Code/Term Type

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

Meniscus prosthesis Meniscus prosthesis Class IIb

Arthroscopic surgical procedure kit non-medicated reusable Arthroscopic surgical procedure kit non-medicated 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
Orthopaedic surgical procedure kit non-medicated single-use	Orthopaedic surgical procedure kit non-medicated single-use	Class IIa
Meniscus prosthesis	Meniscus prosthesis	Class IIb
Arthroscopic surgical procedure kit non-medicated reusable	Arthroscopic surgical procedure kit non-medicated reusable	Class I