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.
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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
Relationship Type
Address
6 Wilmslow Road, Rusholme
Manchester, England, United Kingdom
Postcode: M14 5TP
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Flexible endoscopic biopsy handpiece/needle
Type: General Medical Device
Manufacturer: Finemedix Co., Ltd.