Soft corrective contact lens, daily-wear - UK MHRA Medical Device Registration

Soft corrective contact lens, daily-wear is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 181241. The device is manufactured by Gelflex from Australia, classified as General Medical Device. The authorized representative in the UK is UK RepMed 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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Soft corrective contact lens, daily-wear

MHRA Device ID: 181241•Ref: 181241

Device Type

General Medical Device

Devices

Soft corrective contact lens, daily-wear

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 15, 2024

Manufacturer Information

Name

Gelflex

Address

52 Mulgul Road Malaga Perth Western Austailia

Perth, Australia

Created Date

Nov 3, 2023

Authorized Representative

Name

UK RepMed Ltd.

Relationship Type

UK Responsible Person

Address

Unit D, Crondall Place Coxbridge Business Park Alton Road Farnham, Surrey,

Farnham, England, United Kingdom

Postcode: GU10 5EH

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Other Products from Gelflex (1)

Soft corrective contact lens, daily-disposable

Type: General Medical Device

Registered: Nov 26, 2024

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Soft corrective contact lens, daily-wear - UK MHRA Medical Device Registration

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