Fistula needle, single-use - UK MHRA Medical Device Registration
Fistula needle, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 92682. The device is manufactured by Guangdong Baihe Medical Technology Co., Ltd from China, classified as General Medical Device. The authorized representative in the UK is CMC Medical Devices 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
Fistula needle, single-use
Type
Class IIa
Date Registered
Jun 3, 2024
Last Updated
Oct 4, 2023
Address
No.89, Taoyuan East Road, Nanhai, Foshan, Guangdong Province, P.R. China
Fo Shan, China
Created Date
Aug 6, 2021
Relationship Type
Address
Office 32 19-21 Crawford Street
London, United Kingdom
Postcode: W1H 1PJ
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