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 191771. The device is manufactured by i-SENS, Inc. from South Korea, classified as General Medical Device. The authorized representative in the UK is MT Promedt Consulting Ltd.

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Percutaneous interstitial-fluid glucose monitoring system, electrochemical

MHRA Device ID: 191771•Ref: 191771

Device Type

General Medical Device

Devices

Percutaneous interstitial-fluid glucose monitoring system, electrochemical

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

May 9, 2024

Manufacturer Information

Name

i-SENS, Inc.

Address

43, Banpo-daero 28-gil, Seocho-gu

Seoul , South Korea

Created Date

Jul 21, 2021

Authorized Representative

Name

MT Promedt Consulting Ltd

Relationship Type

UK Responsible Person

Address

Beaver House, 23-38 Hythe Bridge Street

Oxford, England, United Kingdom

Postcode: OX1 2EP

DJ Fang

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

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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