Pure Global

ERCP catheter, balloon, electrosurgical, sphincter-dilation - UK MHRA Medical Device Registration

ERCP catheter, balloon, electrosurgical, sphincter-dilation is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 110870. The device is manufactured by Medi-Globe GmbH from Germany, classified as General Medical Device. The authorized representative in the UK is Qserve Group 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.

Free Database
Powered by Pure Global AI
MHRA Registered
General Medical Device
๐Ÿ‡ฌ๐Ÿ‡ง
ERCP catheter, balloon, electrosurgical, sphincter-dilation
MHRA Device ID: 110870โ€ขRef: 110870

Device Type

General Medical Device

Devices

ERCP catheter, balloon, electrosurgical, sphincter-dilation

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Address

Medi-Globe StraรŸe 1-5

Achenmรผhle, Germany

Created Date

Apr 13, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing