United Kingdom MHRA device registration 205988

Percutaneous interstitial-fluid glucose monitoring system, electrochemical

United Kingdom·General Medical Device·Medtronic MINIMED·Registered Jan 29, 2025DREGIY

Registration details

Device ID: 205988
Status: DREGIY
Date Registered: Jan 29, 2025

Device classification

Device Type: General Medical Device
Type: Class IIb

Manufacturer

Name: Medtronic MINIMED
Address: 1800 Devonshire Street
Northridge, United States

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About this record

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 205988. The device is manufactured by Medtronic MINIMED from United States, classified as General Medical Device.

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