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 - Datex-Ohmeda Inc

Address:

9900 Innovation Drive

Wauwatosa

53226

United States

Authorised Representative/ UK Responsible Person
Name: GE Medical Systems Limited
Address:

Pollards Wood Nightingales Lane Buckinghamshire

Chalfont St Giles

HP8 4SP

England United Kingdom

Code/Term Type

General-purpose patient temperature probe reusable General-purpose patient temperature probe reusable Class I

Conventional infant incubator Conventional infant incubator 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
General-purpose patient temperature probe reusable	General-purpose patient temperature probe reusable	Class I
Conventional infant incubator	Conventional infant incubator	Class IIb