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 94021. The device is manufactured by Cytophil, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is QCS International LTD..

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General-purpose endoscopic needle, single-use

MHRA Device ID: 94021•Ref: 94021

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

Cytophil, Inc.

Address

2485 Corporate Circle Suite 2

East Troy, WI, United States

Created Date

Apr 30, 2021

Authorized Representative

Name

QCS International LTD.

Relationship Type

UK Responsible Person

Address

Suite 9 Cumbernauld Business Park Wardpark Road

Cumbernauld, North Lanarkshire, Scotland, United Kingdom

Postcode: G67 3JZ

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

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