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 - INVAMED SAGLIK ILAC SAN VE TIC AS

Address:

Alci OSB Mahallesi ASO 2 OSB 2010. Cd. No:4 Malikoy Anadolu Osb Sincan

ANKARA

06930

Turkey

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

S&F Reform Road

Clyde House

Maidenhead

Berkshire SL6 8BY

England United Kingdom

Code/Term Type

Varicose vein adhesive-treatment kit Varicose vein adhesive-treatment kit Class III

Peripheral angioplasty balloon catheter drug-coated Peripheral angioplasty balloon catheter drug-coated Class III

Neurovascular embolization coil Neurovascular embolization coil 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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Code/Term		Type
Varicose vein adhesive-treatment kit	Varicose vein adhesive-treatment kit	Class III
Peripheral angioplasty balloon catheter drug-coated	Peripheral angioplasty balloon catheter drug-coated	Class III
Neurovascular embolization coil	Neurovascular embolization coil	Class III