Endoscopic biopsy valve, single-use - UK MHRA Medical Device Registration
Endoscopic biopsy valve, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 124114. The device is manufactured by FUJIFILM Corporation from Japan, classified as General Medical Device. The authorized representative in the UK is Fujifilm Healthcare UK 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.
Device Type
General Medical Device
Devices
Endoscopic biopsy valve, single-use
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Apr 20, 2024
Address
26-30 Nishiazabu 2-chome Minato-ku
Tokyo, Japan
Created Date
Sep 27, 2021
Relationship Type
Address
Fujifilm House Whitbread Way
Bedford, England, United Kingdom
Postcode: MK42 0ZE
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