Eye pad - UK MHRA Medical Device Registration

Eye pad is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 93301. The device is manufactured by ALLMED Medical Products Co., Ltd. from China, classified as General Medical Device. The authorized representative in the UK is SUNGO Certification Company 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.

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Eye pad

MHRA Device ID: 93301•Ref: 93301

Device Type

General Medical Device

Devices

Eye pad

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Jun 20, 2024

Manufacturer Information

Name

ALLMED Medical Products Co., Ltd.

Address

No.18 Qixing Road, Majiadian Town, Zhijiang City

Hubei Province, China

Created Date

Jul 7, 2021

Authorized Representative

Name

SUNGO Certification Company Limited

Relationship Type

UK Responsible Person

Address

3rd Floor, 70 Gracechurch Street

London, England, United Kingdom

Postcode: EC3V 0HR

DJ Fang

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Other Products from ALLMED Medical Products Co., Ltd. (10)

Other Products from Same Authorized Representative (10)

Eye pad - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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Eye pad