Manual blood lancing device, single-use - UK MHRA Medical Device Registration
Manual blood lancing device, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 197834. The device is manufactured by TaiDoc Technology Corp from Taiwan, classified as General Medical Device. The authorized representative in the UK is Medimap 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.
Device Type
General Medical Device
Devices
Manual blood lancing device, single-use
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Sep 13, 2024
Address
B1-7F, No 127 Wugong 2nd Road
New Taipei City, Wugu Dist, Taiwan
Created Date
Sep 7, 2021
Name
Medimap LtdRelationship Type
Address
2 The Drift
Thurston, Suffolk, United Kingdom
Postcode: IP31 3RT
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