Nephrostomy catheter - UK MHRA Medical Device Registration

Nephrostomy catheter is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 96057. The device is manufactured by UreSil, LLC from United States, 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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Nephrostomy catheter

MHRA Device ID: 96057•Ref: 96057

Device Type

General Medical Device

Devices

Nephrostomy catheter

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jul 3, 2024

Manufacturer Information

Name

UreSil, LLC

Address

5418 W Touhy Ave

Skokie, Illinois, United States

Created Date

Aug 18, 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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Nephrostomy catheter - UK MHRA Medical Device Registration

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Date Registered

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