Nitrile examination/treatment glove, non-powdered, non-antimicrobial - UK MHRA Medical Device Registration
Nitrile examination/treatment glove, non-powdered, non-antimicrobial is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 98735. The device is manufactured by Akisa (HK) Co Ltd from China, 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
Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Type
Class I
Date Registered
Aug 25, 2021
Last Updated
Dec 22, 2022
Address
Unit 04 7/F Brightway Tower No33 Mongkok Road
Hong Kong, Kowloon, China
Created Date
Aug 25, 2021
Name
Medimap LtdRelationship Type
Address
2 The Drift
Thurston, Suffolk, United Kingdom
Postcode: IP31 3RT
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