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 - OSI Optoelectronics Inc.

Address:

12525 Chadron Avenue

Hawthorne

California 90250

United States

Authorised Representative/ UK Responsible Person
Name: QCS International LTD.
Address:

Suite 9 Cumbernauld Business Park

Wardpark Road

Cumbernauld

North Lanarkshire G67 3JZ

Scotland United Kingdom

Code/Term Type

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

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