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

Back to MHRA

Manufacturer's Devices - Meditech International Inc.

Address:

411 Horner Avenue Unit 1

Ontario

M8W 4W3

Canada

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

Sandford Gate East Point Business Park

Oxford

OX4 6LB

England United Kingdom

Code/Term Type

Red-light phototherapy unit professional Red-light phototherapy unit professional Class IIb

Red-light phototherapy unit professional Red-light phototherapy unit professional 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
Red-light phototherapy unit professional	Red-light phototherapy unit professional	Class IIb
Red-light phototherapy unit professional	Red-light phototherapy unit professional	Class IIa