Percutaneous interstitial-fluid glucose monitoring system, electrochemical - UK MHRA Medical Device Registration
Percutaneous interstitial-fluid glucose monitoring system, electrochemical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 181627. The device is manufactured by Changsha Sinocare Inc. from China, classified as General Medical Device. The authorized representative in the UK is SUNGO Certification Company Limited.
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
Percutaneous interstitial-fluid glucose monitoring system, electrochemical
Type
Class IIb
Date Registered
Nov 26, 2024
Last Updated
Mar 13, 2024
Address
No. 265 Guyuan Road, Hi-tech Zone, Changsha
Hunan Province, China
Created Date
May 25, 2021
Relationship Type
Address
3rd Floor, 70 Gracechurch Street
London, England, United Kingdom
Postcode: EC3V 0HR
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