United Kingdom MHRA device registration 95725

Flexible endoscopic biopsy forceps, single-use

United Kingdom·General Medical Device·Finemedix Co., Ltd.·Registered Aug 18, 2021

Registration details

Device ID: 95725
MHRA Reference Number: 95725
Date Registered: Aug 18, 2021
Last Updated: Oct 13, 2022

Device classification

Device Type: General Medical Device
Devices: Flexible endoscopic biopsy forceps, single-use
Type: Class IIa

Manufacturer

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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About this record

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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