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 100554. The device is manufactured by United States Endoscopy Group, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is STERIS Solutions 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
Flexible endoscopic biopsy forceps, single-use
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
May 2, 2024
Address
5976 Heisley Road
Mentor, Ohio, United States
Created Date
Jun 30, 2021
Relationship Type
Address
Chancery House, Rayns Way Watermead Business Park Syston
Leicester, Leicestershire, England, United Kingdom
Postcode: LE7 1PF
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