United Kingdom MHRA device registration 101619

Percutaneous interstitial-fluid glucose monitoring system, electrochemical

United Kingdom·General Medical Device·DexCom, Inc.·Registered Aug 11, 2024

Registration details

Device ID: 101619
MHRA Reference Number: 101619
Date Registered: Aug 11, 2024
Last Updated: Oct 10, 2023

Device classification

Device Type: General Medical Device
Devices: Percutaneous interstitial-fluid glucose monitoring system, electrochemical
Type: Class IIb

Manufacturer

Name: DexCom, Inc.
Address: 6340 Sequence Drive
San Diego, CA, United States
Created Date: Aug 31, 2021

Authorized Representative

Name: MDSS-UK RP LIMITED
Relationship Type: UK Responsible Person
Address: 6 Wilmslow Road, Rusholme
Manchester, England, United Kingdom
Postcode: M14 5TP

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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 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.

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