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 - DANAMECO MEDICAL JOINT STOCK CORPORATION

Address:

12 Trinh Cong Son Street Hoa Cuong Nam Ward

Da Nang City

Hai Chau District 50218

Vietnam

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

Patient surgical drape single-use Patient surgical drape single-use Class I

Woven gauze pad non-sterile Woven gauze pad non-sterile Class I

Isolation gown single-use Isolation gown single-use Class I

Surgical/medical face mask single-use Surgical/medical face mask 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
Patient surgical drape single-use	Patient surgical drape single-use	Class I
Woven gauze pad non-sterile	Woven gauze pad non-sterile	Class I
Isolation gown single-use	Isolation gown single-use	Class I
Surgical/medical face mask single-use	Surgical/medical face mask single-use	Class I