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 - Fazzini s.r.l

Address:

Padana Superiore 317 - 20055 - Vimodrone (MI) Italy.

Milan

Vimodrone 20055

Italy

Authorised Representative/ UK Responsible Person
Name: Therapy Equipment Ltd
Address:

Unit 1 Cranbourne Avenue Cranbourne Industrial Estate

Potters Bar

Herts EN6 3JN

United Kingdom

Code/Term Type

Surgical suction system collection container reusable Surgical suction system collection container reusable Class I

Suction system canister liner Suction system canister liner Class I

General-purpose surgical suction system electric General-purpose surgical suction system electric Class IIa

Benchtop nebulizer non-heated Benchtop nebulizer non-heated Class IIa

Ultrasonic nebulizing system Ultrasonic nebulizing system 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
Surgical suction system collection container reusable	Surgical suction system collection container reusable	Class I
Suction system canister liner	Suction system canister liner	Class I
General-purpose surgical suction system electric	General-purpose surgical suction system electric	Class IIa
Benchtop nebulizer non-heated	Benchtop nebulizer non-heated	Class IIa
Ultrasonic nebulizing system	Ultrasonic nebulizing system	Class IIa