Eye anterior segment analyser - UK MHRA Medical Device Registration

Eye anterior segment analyser is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 177887. The device is manufactured by Konan Medical, Inc. from Japan, classified as General Medical Device. The authorized representative in the UK is MT Promedt Consulting 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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Eye anterior segment analyser

MHRA Device ID: 177887•Ref: 177887

Device Type

General Medical Device

Devices

Eye anterior segment analyser

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Mar 19, 2024

Manufacturer Information

Name

Konan Medical, Inc.

Address

10-29, Miyanishicho

Nishinomiya, Hyogo, Japan

Created Date

May 27, 2021

Authorized Representative

Name

MT Promedt Consulting Ltd

Relationship Type

UK Responsible Person

Address

Beaver House, 23-38 Hythe Bridge Street

Oxford, England, United Kingdom

Postcode: OX1 2EP

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Eye anterior segment analyser - UK MHRA Medical Device Registration

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