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 - Bioengineering Laboratories Srl

Address:

Via Antonio Vivaldi 32/A

Cantù

Como 22063

Italy

Authorised Representative/ UK Responsible Person
Name: Donawa Lifescience Ltd
Address:

Aviation Business Park Enterprise Close

Christchurch

BH23 6NX

England United Kingdom

Code/Term Type

Gastrointestinal motility manometric catheter non-electronic Gastrointestinal motility manometric catheter non-electronic Class IIa

Urodynamic manometric catheter non-electronic Urodynamic manometric catheter non-electronic Class IIa

Intra-abdominal pressure measurement set mechanical Intra-abdominal pressure measurement set mechanical 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
Gastrointestinal motility manometric catheter non-electronic	Gastrointestinal motility manometric catheter non-electronic	Class IIa
Urodynamic manometric catheter non-electronic	Urodynamic manometric catheter non-electronic	Class IIa
Intra-abdominal pressure measurement set mechanical	Intra-abdominal pressure measurement set mechanical	Class I