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 95725. The device is manufactured by Finemedix Co., Ltd. from South Korea, classified as General Medical Device. The authorized representative in the UK is MDSS-UK RP 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: 95725•Ref: 95725

Device Type

General Medical Device

Devices

Flexible endoscopic biopsy forceps, single-use

Type

Class IIa

Date Registered

Aug 18, 2021

Last Updated

Oct 13, 2022

Manufacturer Information

Name

Finemedix Co., Ltd.

Address

140-9, Yuram-ro

Dong-gu, Daegu, South Korea

Created Date

Aug 18, 2021

Authorized Representative

Name

MDSS-UK RP LIMITED

Relationship Type

UK Responsible Person

Address

6 Wilmslow Road, Rusholme

Manchester, England, United Kingdom

Postcode: M14 5TP

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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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Created Date

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Address

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