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 - Intersurgical SpA

Address:

Via Morandi 12

Mirandola

41037

Italy

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

Crane House Molly Millars Lane

Wokingham

Berkshire RG41 2RZ

England United Kingdom

Code/Term Type

Straight/elbow breathing circuit connector single-use Straight/elbow breathing circuit connector single-use Class I

Oxygen administration tent adult Oxygen administration tent adult Class IIa

PEEP valve reusable PEEP valve reusable Class IIa

Venturi oxygen face mask Venturi oxygen face mask Class IIa

Venturi oxygen face mask Venturi oxygen face mask 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
Straight/elbow breathing circuit connector single-use	Straight/elbow breathing circuit connector single-use	Class I
Oxygen administration tent adult	Oxygen administration tent adult	Class IIa
PEEP valve reusable	PEEP valve reusable	Class IIa
Venturi oxygen face mask	Venturi oxygen face mask	Class IIa
Venturi oxygen face mask	Venturi oxygen face mask	Class IIa