United Kingdom MHRA device registration 148402

Ultrasound endoscope balloon, synthetic polymer

United Kingdom flagUnited Kingdom·General Medical Device·United States Endoscopy Group, Inc.·Registered Nov 26, 2024
Registration details
Device ID
148402
MHRA Reference Number
148402
Date Registered
Nov 26, 2024
Last Updated
May 2, 2024
Device classification
Device Type
General Medical Device
Devices
Ultrasound endoscope balloon, synthetic polymer
Type
Class I
Manufacturer
Address
5976 Heisley Road
Mentor, Ohio, United States
Created Date
Jun 30, 2021
Authorized Representative
Relationship Type
UK Responsible Person
Address
Chancery House, Rayns Way Watermead Business Park Syston
Leicester, Leicestershire, England, United Kingdom
Postcode: LE7 1PF
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About this record

Ultrasound endoscope balloon, synthetic polymer is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 148402. 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.

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