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 209933. The device is manufactured by Medtronic MINIMED from United States, classified as System or Procedure Pack.
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Device Type
System or Procedure Pack
Type
System or Procedure Pack
Status
Date Registered
Feb 1, 2025
Address
1800 Devonshire Street
Northridge, United States
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Percutaneous interstitial-fluid glucose monitoring system, electrochemical
Type: General Medical Device
Registered: Jan 29, 2025
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Type: General Medical Device
Registered: Nov 26, 2024
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Type: General Medical Device
Registered: Nov 26, 2024
Percutaneous interstitial-fluid glucose monitoring system needle electrode
Type: General Medical Device
Registered: Nov 26, 2024
Percutaneous interstitial-fluid glucose monitoring system needle electrode
Type: General Medical Device
Registered: Nov 26, 2024
Hypoallergenic skin adhesive tape
Type: General Medical Device
Registered: Nov 26, 2024

