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 - Hantech Medical Device Co. Ltd.

Address:

No.288 Sanheng Road Changhe Industrial Park

Cixi

Ningbo

Zhejiang Province 315326

China

Authorised Representative/ UK Responsible Person
Name: NPZ technology Ltd
Address:

Stirling House Cambridge Innovation Park

Denny End Road Waterbeach

Cambridge

Cambridgeshire CB25 9QE

United Kingdom

Code/Term Type

Umbilical cord clip Umbilical cord clip Class I

Umbilical cord clamp remover Umbilical cord clamp remover Class I

Amniotic membrane perforator single-use Amniotic membrane perforator single-use Class IIa

Amniotic membrane perforator single-use Amniotic membrane perforator single-use 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
Umbilical cord clip	Umbilical cord clip	Class I
Umbilical cord clamp remover	Umbilical cord clamp remover	Class I
Amniotic membrane perforator single-use	Amniotic membrane perforator single-use	Class IIa
Amniotic membrane perforator single-use	Amniotic membrane perforator single-use	Class I