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 - Akzenta International SA

Address:

Via Giuseppe Motta 24

Chiasso

CH-6830

Switzerland

Authorised Representative/ UK Responsible Person
Name: MDQ Services Ltd
Address:

Flat 81 Seacon Tower 5 Hutching’s Street

London

England E14 8JX

England United Kingdom

Code/Term Type

Surgical/medical face mask antimicrobial single-use Surgical/medical face mask antimicrobial single-use Class I

General-purpose absorbent tip applicator/swab single-use General-purpose absorbent tip applicator/swab single-use Class I

Nitrile examination/treatment glove non-powdered non-antimicrobial Nitrile examination/treatment glove non-powdered non-antimicrobial Class I

Hevea-latex examination/treatment glove non-powdered non-antimicrobial Hevea-latex examination/treatment glove non-powdered non-antimicrobial 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
Surgical/medical face mask antimicrobial single-use	Surgical/medical face mask antimicrobial single-use	Class I
General-purpose absorbent tip applicator/swab single-use	General-purpose absorbent tip applicator/swab single-use	Class I
Nitrile examination/treatment glove non-powdered non-antimicrobial	Nitrile examination/treatment glove non-powdered non-antimicrobial	Class I
Hevea-latex examination/treatment glove non-powdered non-antimicrobial	Hevea-latex examination/treatment glove non-powdered non-antimicrobial	Class I