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 - Auckland Medical Polymer (Tianjin) Co. Ltd.

Address:

Building D5-2 XEDA International Industrial Park Xiqing Economic Development Area (XEDA)

Tianjin

300385

China

Authorised Representative/ UK Responsible Person
Name: KINGSMEAD SERVICE LIMITED
Address:

19 MEZZANINE FLOOR 19-21 CRAWFORD STREET

London

W1H 1PJ

England United Kingdom

Code/Term Type

Electrosurgical return electrode reusable Electrosurgical return electrode reusable Class I

Freestanding patient positioner reusable Freestanding patient positioner reusable Class I

Leg intraoperative repositioning support Leg intraoperative repositioning support Class I

Intravenous pole Intravenous pole Class I

Intravenous pole Intravenous pole 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
Electrosurgical return electrode reusable	Electrosurgical return electrode reusable	Class I
Freestanding patient positioner reusable	Freestanding patient positioner reusable	Class I
Leg intraoperative repositioning support	Leg intraoperative repositioning support	Class I
Intravenous pole	Intravenous pole	Class I
Intravenous pole	Intravenous pole	Class I