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 - Lumitex Medical Devices Inc.

Address:

8443 Dow Circle

Strongsville OH

44136

United States

Authorised Representative/ UK Responsible Person
Name: MDSS-UK RP LIMITED
Address:

6 Wilmslow Road Rusholme

Manchester

M14 5TP

England United Kingdom

Code/Term Type

Blanket/pad infant phototherapy unit Blanket/pad infant phototherapy unit Class IIa

Phototherapy infant blanket Phototherapy infant blanket Class I

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
Blanket/pad infant phototherapy unit	Blanket/pad infant phototherapy unit	Class IIa
Phototherapy infant blanket	Phototherapy infant blanket	Class I