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 - MENTOR MEDICAL SYSTEMS B.V.

Address:

ZERNIKEDREEF 2

CL LEIDEN

2333

Netherlands

Authorised Representative/ UK Responsible Person
Name: Johnson & Johnson Medical Ltd
Address:

Baird House 4 Lower Gilmore Bank

Edinburgh

EH3 9QP

Scotland United Kingdom

Code/Term Type

Silicone gel/saline-filled breast implant Silicone gel/saline-filled breast implant 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

Invasive breast implant sizer fixed reusable Invasive breast implant sizer fixed reusable 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
Silicone gel/saline-filled breast implant	Silicone gel/saline-filled breast implant	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
Invasive breast implant sizer fixed reusable	Invasive breast implant sizer fixed reusable	Class IIa