Amniotic membrane perforator, single-use - UK MHRA Medical Device Registration

Amniotic membrane perforator, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 156414. The device is manufactured by Hantech Medical Device Co., Ltd. from China, classified as General Medical Device. The authorized representative in the UK is NPZ technology Ltd.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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Amniotic membrane perforator, single-use

MHRA Device ID: 156414•Ref: 156414

Device Type

General Medical Device

Devices

Amniotic membrane perforator, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jan 13, 2024

Manufacturer Information

Name

Hantech Medical Device Co., Ltd.

Address

No.288 Sanheng Road Changhe Industrial Park Cixi

Ningbo, Zhejiang Province, China

Created Date

Sep 21, 2022

Authorized Representative

Name

NPZ technology Ltd

Relationship Type

UK Responsible Person

Address

Stirling House Cambridge Innovation Park, Denny End Road, Waterbeach

Cambridge, Cambridgeshire, United Kingdom

Postcode: CB25 9QE

DJ Fang

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Other Products from Hantech Medical Device Co., Ltd. (5)

Other Products from Same Authorized Representative (10)

Amniotic membrane perforator, single-use - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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