Endoscopic overtube, single-use - UK MHRA Medical Device Registration

Endoscopic overtube, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 199900. The device is manufactured by Endo Tools Therapeutics S.A. from Belgium, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (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.

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Endoscopic overtube, single-use

MHRA Device ID: 199900•Ref: 199900

Device Type

General Medical Device

Devices

Endoscopic overtube, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Sep 26, 2024

Manufacturer Information

Name

Endo Tools Therapeutics S.A.

Address

Rue Auguste Piccard 48

Gosselies, Belgium

Created Date

Aug 12, 2021

Authorized Representative

Name

Emergo Consulting (UK) Limited

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 – UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

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Other Products from Endo Tools Therapeutics S.A. (3)

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Endoscopic overtube, single-use - UK MHRA Medical Device Registration

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