Gastrointestinal/biliary dilation balloon catheter - UK MHRA Medical Device Registration
Gastrointestinal/biliary dilation balloon catheter is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 117131. The device is manufactured by PENTAX of the Americas, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Pentax UK Ltd.
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
Gastrointestinal/biliary dilation balloon catheter
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Oct 22, 2024
Address
3 Paragon Drive
Montvale, United States
Created Date
Dec 2, 2021
Name
Pentax UK LtdRelationship Type
Address
Unit D1 Heron Drive Langley
Slough, Berks, England, United Kingdom
Postcode: sl3 8pn
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