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..
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.
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
Name
Cytophil, Inc.Address
2485 Corporate Circle Suite 2
East Troy, WI, United States
Created Date
Apr 30, 2021
Relationship Type
Address
Suite 9 Cumbernauld Business Park Wardpark Road
Cumbernauld, North Lanarkshire, Scotland, United Kingdom
Postcode: G67 3JZ
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