General-purpose endoscopic needle, single-use - UK MHRA Medical Device Registration

General-purpose endoscopic needle, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 75239. The device is manufactured by Uroplasty LLC from United States, 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.

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General-purpose endoscopic needle, single-use

MHRA Device ID: 75239•Ref: 75239

Device Type

General Medical Device

Devices

General-purpose endoscopic needle, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

Uroplasty LLC

Address

5420 Feltl Road

Minnetonka, Minnesota , United States

Created Date

Apr 23, 2021

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

DJ Fang

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General-purpose endoscopic needle, single-use - UK MHRA Medical Device Registration

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