Urological fluid funnel - UK MHRA Medical Device Registration

Urological fluid funnel is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 153057. The device is manufactured by TIDI Product, 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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Urological fluid funnel

MHRA Device ID: 153057•Ref: 153057

Device Type

General Medical Device

Devices

Urological fluid funnel

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Nov 6, 2024

Manufacturer Information

Name

TIDI Product, LLC

Address

570 Enterprise Drive

Neenah, Wisconsin, United States

Created Date

Nov 5, 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 TIDI Product, LLC (10)

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Urological fluid funnel - UK MHRA Medical Device Registration

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Type

Date Registered

Last Updated

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Address

Created Date

Name

Relationship Type

Address

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