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 - G & G Biotechnology Ltd

Address:

4 Ben Gurion Street

Haifa

3541415

Israel

Authorised Representative/ UK Responsible Person
Name: Medimap Ltd
Address:

2 The Drift

Thurston

Suffolk IP31 3RT

United Kingdom

Code/Term Type

Silicone gel-filled breast implant polyurethane-foam-surface Silicone gel-filled breast implant polyurethane-foam-surface Class III

Silicone gel-filled breast implant smooth-surface Silicone gel-filled breast implant smooth-surface Class III

Silicone gel-filled breast implant textured-surface Silicone gel-filled breast implant textured-surface Class III

Gluteal implant Gluteal implant Class IIb

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
Silicone gel-filled breast implant polyurethane-foam-surface	Silicone gel-filled breast implant polyurethane-foam-surface	Class III
Silicone gel-filled breast implant smooth-surface	Silicone gel-filled breast implant smooth-surface	Class III
Silicone gel-filled breast implant textured-surface	Silicone gel-filled breast implant textured-surface	Class III
Gluteal implant	Gluteal implant	Class IIb