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 - GF Health Products Inc.

Address:

1 Graham Field Way

Atlanta

Georgia 30340

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

Hospital stretcher manual Hospital stretcher manual Class I

Hospital stretcher powered Hospital stretcher powered Class I

General examination/treatment chair electric General examination/treatment chair electric Class I

Operating room stool Operating room stool Class I

General examination/treatment chair manual General examination/treatment chair manual 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
Hospital stretcher manual	Hospital stretcher manual	Class I
Hospital stretcher powered	Hospital stretcher powered	Class I
General examination/treatment chair electric	General examination/treatment chair electric	Class I
Operating room stool	Operating room stool	Class I
General examination/treatment chair manual	General examination/treatment chair manual	Class I