Pure Global

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 181869. The device is manufactured by Shenzhen SiSensing Co., Ltd. from China, classified as General Medical Device. The authorized representative in the UK is KINGSMEAD SERVICE LIMITED.

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.

Free Database
Powered by Pure Global AI
MHRA Registered
General Medical Device
๐Ÿ‡ฌ๐Ÿ‡ง
Percutaneous interstitial-fluid glucose monitoring system, electrochemical
MHRA Device ID: 181869โ€ขRef: 181869

Device Type

General Medical Device

Devices

Percutaneous interstitial-fluid glucose monitoring system, electrochemical

Type

Class IIb

Date Registered

Sep 8, 2024

Last Updated

Aug 20, 2024

Manufacturer Information

Address

Room 901, Building No.3, Tinwe Business Park, No.6 Liufang Road, Xingdong Community, Xinan Street, Baoan District

Shenzhen, Guangdong, China

Created Date

Nov 15, 2023

Authorized Representative

Relationship Type

UK Responsible Person

Address

19 MEZZANINE FLOOR 19-21 CRAWFORD STREET

London, England, United Kingdom

Postcode: W1H 1PJ

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing