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 - Codonics Inc.

Address:

17991 Englewood Drive

Middleburg Heights

Ohio 44130

United States

Authorised Representative/ UK Responsible Person
Name: UKCApartner4U Limited
Address:

7 CAMPION WAY

BINGHAM NOTTINGHAM

NG13 8 TR

England United Kingdom

Code/Term Type

Medication management system Medication management system Class I

Medical printer film Medical printer film Class I

DICOM image data disc-recording unit DICOM image data disc-recording unit 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
Medication management system	Medication management system	Class I
Medical printer film	Medical printer film	Class I
DICOM image data disc-recording unit	DICOM image data disc-recording unit	Class I