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 - Garware Fulflex India Private Limited

Address:

Plot No C2 D28 MIDC

Satara District

Wai

Maharashtra 412803

India

Authorised Representative/ UK Responsible Person
Name: ALS International Ltd Trading as I3CGLOBAL(UK)
Address:

Office 54 58 Peregrine Road

Hainault

Ilford

Essex IG6 3SZ

England United Kingdom

Code/Term Type

Pressure bandage non-latex single-use Pressure bandage non-latex single-use Class I

Limb tourniquet manual single-use Limb tourniquet manual single-use 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
Pressure bandage non-latex single-use	Pressure bandage non-latex single-use	Class I
Limb tourniquet manual single-use	Limb tourniquet manual single-use	Class I