Soft corrective contact lens, daily-wear
United Kingdom·General Medical Device·Gelflex·Registered Nov 26, 2024- Device ID
- 181241
- MHRA Reference Number
- 181241
- Date Registered
- Nov 26, 2024
- Last Updated
- Oct 15, 2024
- Device Type
- General Medical Device
- Devices
- Soft corrective contact lens, daily-wear
- Type
- Class IIa
- Name
- Gelflex
- Address
- 52 Mulgul Road Malaga Perth Western Austailia Perth, Australia
- Created Date
- Nov 3, 2023
- Name
- UK RepMed Ltd.
- Relationship Type
- UK Responsible Person
- Address
- Unit D, Crondall Place Coxbridge Business Park Alton Road Farnham, Surrey, Farnham, England, United KingdomPostcode: GU10 5EH
Devices with a matching generic name or device type registered with MHRA
Additional devices registered by the same manufacturer
Additional devices represented by UK RepMed Ltd. in the UK
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.