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 - EURONDA S.P.A.

Address:

Via dell’Artigianato 7

Montecchio Precalcino (Vi)

36030

Italy

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

Pure Offices Plato Close

Warwick

CV34 6WE

England United Kingdom

Code/Term Type

Steam sterilizer Steam sterilizer Class IIb

Endothermic cold therapy pack Endothermic cold therapy pack Class IIa

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

Dental suction system cannula single-use Dental suction system cannula single-use Class IIa

Sterilization packaging single-use Sterilization packaging single-use Class I

Dental cotton roll Dental cotton roll Class I

Dental suction system cannula reusable Dental suction system cannula 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
Steam sterilizer	Steam sterilizer	Class IIb
Endothermic cold therapy pack	Endothermic cold therapy pack	Class IIa
Surgical/medical face mask single-use	Surgical/medical face mask single-use	Class I
Dental suction system cannula single-use	Dental suction system cannula single-use	Class IIa
Sterilization packaging single-use	Sterilization packaging single-use	Class I
Dental cotton roll	Dental cotton roll	Class I
Dental suction system cannula reusable	Dental suction system cannula reusable	Class IIa