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 86941. The device is manufactured by Medtronic MINIMED from United States, classified as General Medical Device. The authorized representative in the UK is Medtronic Limited.

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Percutaneous interstitial-fluid glucose monitoring system, electrochemical

MHRA Device ID: 86941•Ref: 86941

Device Type

General Medical Device

Devices

Percutaneous interstitial-fluid glucose monitoring system, electrochemical

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Apr 9, 2024

Manufacturer Information

Name

Medtronic MINIMED

Address

1800 Devonshire Street

Northridge, United States

Created Date

Jun 30, 2021

Authorized Representative

Name

Medtronic Limited

Relationship Type

UK Responsible Person

Address

Building 9 Croxley Park

Watford, Herts, England, United Kingdom

Postcode: WD18 8WW

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

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Date Registered

Last Updated

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Created Date

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Address

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