Endoscope antifog solution - UK MHRA Medical Device Registration

Endoscope antifog solution is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 89051. The device is manufactured by Unimax Medical Systems Inc. from Taiwan, classified as General Medical Device. The authorized representative in the UK is Qserve Group UK, 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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Endoscope antifog solution

MHRA Device ID: 89051•Ref: 89051

Device Type

General Medical Device

Devices

Endoscope antifog solution

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

Unimax Medical Systems Inc.

Address

8F-2,No. 127, Lane 235, Pao Chiao Road

New Taipei City, Xindian Dist., Taiwan

Created Date

Jul 15, 2021

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

DJ Fang

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Other Products from Unimax Medical Systems Inc. (9)

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Endoscope antifog solution - 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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