United Kingdom MHRA device registration 191771

Percutaneous interstitial-fluid glucose monitoring system, electrochemical

United Kingdom·General Medical Device·i-SENS, Inc.·Registered Nov 26, 2024

Registration details

Device ID: 191771
MHRA Reference Number: 191771
Date Registered: Nov 26, 2024
Last Updated: May 9, 2024

Device classification

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

Manufacturer

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

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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 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.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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