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 - Rossmax Innotek Corp.

Address:

12F. No.189 Kang Chien Rd.

Taipei

11494

Taiwan

Authorised Representative/ UK Responsible Person
Name: CMC Medical Devices LTD
Address:

Office 32 19-21 Crawford Street

London

W1H 1PJ

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

Pulse oximeter line-powered Pulse oximeter line-powered Class IIb

Pulse oximeter Pulse oximeter 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
Pulse oximeter line-powered	Pulse oximeter line-powered	Class IIb
Pulse oximeter	Pulse oximeter	Class IIb