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 - Gammex Inc.

Address:

7600 Discovery Drive

Middleton WI

53562

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

CT phantom test object CT phantom test object Class I

Laser patient positioning system Laser patient positioning system Class I

Mammographic x-ray phantom test object Mammographic x-ray phantom test object 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
CT phantom test object	CT phantom test object	Class I
Laser patient positioning system	Laser patient positioning system	Class I
Mammographic x-ray phantom test object	Mammographic x-ray phantom test object	Class I