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 - Ashland Specialty Ingredients G.P.

Address:

1005 US HWY 202-206

Bridgewater

New Jersey 08807

United States

Authorised Representative/ UK Responsible Person
Name: Ashland Specialties UK Ltd
Address:

30 Old Bailey

London

Middlesex EC4M 7AU

England United Kingdom

Code/Term Type

Medical x-ray film non-screen Medical x-ray film non-screen Class I

Radiation therapy software Radiation therapy software 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
Medical x-ray film non-screen	Medical x-ray film non-screen	Class I
Radiation therapy software	Radiation therapy software	Class I