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

Hevea-latex 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 82371. The device is manufactured by Careplus (M) Sdn Bhd from Malaysia, classified as General Medical Device. The authorized representative in the UK is Wellkang 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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Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial

MHRA Device ID: 82371•Ref: 82371

Device Type

General Medical Device

Devices

Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Sep 18, 2024

Manufacturer Information

Name

Careplus (M) Sdn Bhd

Address

Lot 120 & 121, Jalan Senawang 3 Senawang Industrial Estate

Seremban, Negeri Sembilan, Malaysia

Created Date

May 25, 2021

Authorized Representative

Name

Wellkang Ltd

Relationship Type

Authorised Representative (Northern Ireland)

Address

Enterprise Hub, NW Business Complex 1 Beraghmore Road

Derry, Northern Ireland, Northern Ireland, United Kingdom

Postcode: BT48 8SE

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Other Products from Careplus (M) Sdn Bhd (1)

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

Type: General Medical Device

Registered: Nov 26, 2024

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

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