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 - Envitec - Wismar GmbH

Address:

Alter Holzhafen 18

Wismar

D-23966

Germany

Authorised Representative/ UK Responsible Person
Name: Viamed Limited
Address:

15 Station Road Cross Hills

Keighley

West Yorkshire BD20 7DT

England United Kingdom

Code/Term Type

Respiratory oxygen monitor line-powered Respiratory oxygen monitor line-powered Class IIa

Respiratory oxygen sensor Respiratory oxygen sensor Class IIa

Pulse oximeter probe reusable Pulse oximeter probe reusable Class IIb

Pulse oximeter Pulse oximeter Class IIb

Pulse oximeter probe single-use Pulse oximeter probe single-use Class IIb

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
Respiratory oxygen monitor line-powered	Respiratory oxygen monitor line-powered	Class IIa
Respiratory oxygen sensor	Respiratory oxygen sensor	Class IIa
Pulse oximeter probe reusable	Pulse oximeter probe reusable	Class IIb
Pulse oximeter	Pulse oximeter	Class IIb
Pulse oximeter probe single-use	Pulse oximeter probe single-use	Class IIb