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 193311. 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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Percutaneous interstitial-fluid glucose monitoring system, electrochemical

MHRA Device ID: 193311•Ref: 193311

Device Type

General Medical Device

Devices

Percutaneous interstitial-fluid glucose monitoring system, electrochemical

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Aug 6, 2024

Manufacturer Information

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

DJ Fang

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Percutaneous interstitial-fluid glucose monitoring system, electrochemical - UK MHRA Medical Device Registration

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Last Updated

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DJ Fang

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Percutaneous interstitial-fluid glucose monitoring system, electrochemical

Percutaneous interstitial-fluid glucose monitoring system, electrochemical

Percutaneous interstitial-fluid glucose monitoring system, electrochemical

Percutaneous interstitial-fluid glucose monitoring system, electrochemical

Percutaneous interstitial-fluid glucose monitoring system, electrochemical

Percutaneous interstitial-fluid glucose monitoring system, electrochemical

Percutaneous interstitial-fluid glucose monitoring system, electrochemical

Percutaneous interstitial-fluid glucose monitoring system, electrochemical

Percutaneous interstitial-fluid glucose monitoring system, electrochemical

Percutaneous interstitial-fluid glucose monitoring system, electrochemical

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