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 101619. The device is manufactured by DexCom, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is MDSS-UK RP 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
Aug 11, 2024
Last Updated
Oct 10, 2023
Relationship Type
Address
6 Wilmslow Road, Rusholme
Manchester, England, United Kingdom
Postcode: M14 5TP
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Type: General Medical Device
Registered: Nov 26, 2024
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Type: General Medical Device
Registered: Nov 26, 2024
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Type: General Medical Device
Registered: Nov 26, 2024
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Type: General Medical Device
Registered: Nov 26, 2024
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Type: General Medical Device
Registered: Aug 31, 2021
Percutaneous interstitial-fluid glucose monitoring system, electrochemical
Type: General Medical Device
Registered: Aug 31, 2021
Percutaneous interstitial-fluid glucose monitoring system, electrochemical
Type: General Medical Device
Registered: Aug 31, 2021
Percutaneous interstitial-fluid glucose monitoring system, electrochemical
Type: General Medical Device
Registered: Aug 31, 2021
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