Flexible endoscopic biopsy forceps, single-use - UK MHRA Medical Device Registration

Flexible endoscopic biopsy forceps, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 199051. The device is manufactured by Hangzhou AGS MedTech Co., Ltd. from China, classified as General Medical Device. The authorized representative in the UK is KINGSMEAD SERVICE LIMITED.

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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Flexible endoscopic biopsy forceps, single-use

MHRA Device ID: 199051•Ref: 199051

Device Type

General Medical Device

Devices

Flexible endoscopic biopsy forceps, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Aug 15, 2024

Manufacturer Information

Name

Hangzhou AGS MedTech Co., Ltd.

Address

Building 2, 5 and 7, No.389 Xingzhong Road, Linping District

Hangzhou, Zhejiang, China

Created Date

May 7, 2021

Authorized Representative

Name

KINGSMEAD SERVICE LIMITED

Relationship Type

UK Responsible Person

Address

19 MEZZANINE FLOOR 19-21 CRAWFORD STREET

London, England, United Kingdom

Postcode: W1H 1PJ

DJ Fang

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Flexible endoscopic biopsy forceps, single-use - UK MHRA Medical Device Registration

Device Type

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Date Registered

Last Updated

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Address

Created Date

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Address

DJ Fang

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