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 94800. The device is manufactured by ConMed Corporation from United States, classified as General Medical Device. The authorized representative in the UK is ConMed 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: 94800•Ref: 94800

Device Type

General Medical Device

Devices

General-purpose endoscopic needle, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Mar 19, 2024

Manufacturer Information

Name

ConMed Corporation

Address

525 French Road

Utica, United States

Created Date

May 18, 2021

Authorized Representative

Name

ConMed UK Ltd

Relationship Type

UK Responsible Person

Address

73/76 Shrivenham Hundred Business Park

Swindon, Wiltshire, England, United Kingdom

Postcode: SN6 8TY

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Other Products from ConMed Corporation (10)

Other Products from Same Authorized Representative (10)

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

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Date Registered

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Created Date

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