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.

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Nitrile examination/treatment glove, non-powdered, non-antimicrobial

MHRA Device ID: 98735•Ref: 98735

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

Manufacturer Information

Name

Akisa (HK) Co Ltd

Address

Unit 04 7/F Brightway Tower No33 Mongkok Road

Hong Kong, Kowloon, China

Created Date

Aug 25, 2021

Authorized Representative

Name

Medimap Ltd

Relationship Type

UK Responsible Person

Address

2 The Drift

Thurston, Suffolk, United Kingdom

Postcode: IP31 3RT

DJ Fang

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Other Products from Akisa (HK) Co Ltd (2)

Vinyl examination/treatment glove, non-powdered

Type: General Medical Device

Registered: Aug 25, 2021

Nitrile examination/treatment glove, non-powdered, non-antimicrobial

Type: General Medical Device

Registered: Aug 25, 2021

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Nitrile examination/treatment glove, non-powdered, non-antimicrobial - UK MHRA Medical Device Registration

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