United Kingdom MHRA device registration 132011

Soft corrective contact lens, daily-wear

United Kingdom·General Medical Device·DreamCon Co., Ltd.·Registered Nov 26, 2024

Registration details

Device ID: 132011
MHRA Reference Number: 132011
Date Registered: Nov 26, 2024
Last Updated: Nov 7, 2023

Device classification

Device Type: General Medical Device
Devices: Soft corrective contact lens, daily-wear
Type: Class IIa

Manufacturer

Name: DreamCon Co., Ltd.
Address: 8, 10, Yeongdong 2-Gil
Yangsan-Si, Gyeongsangnam-Do, South Korea
Created Date: Jan 11, 2022

Authorized Representative

Name: UKCA Experts Ltd.
Relationship Type: UK Responsible Person
Address: Dept 302, 43 Owston Road Carcroft
Doncaster, England, United Kingdom
Postcode: DN6 8DA

Similar products

Devices with a matching generic name or device type registered with MHRA

Manual blood lancing device, single-useN/A

Type: General Medical Device

Manufacturer: Tasso, Inc.

Device ID: 177275

Stationary gamma camera systemN/A

Type: General Medical Device

Manufacturer: GE Medical Systems Israel Functional Imaging

Device ID: 175912

Physiologic monitoring system alarmN/A

Type: General Medical Device

Manufacturer: GE Medical Systems Information Technologies, Inc.

Device ID: 150616

Bedside information system application softwareN/A

Type: General Medical Device

Manufacturer: GE Medical Systems Information Technologies, Inc.

Device ID: 150617

Wireless patient monitor/sensor reporting software, professional-onlyN/A

Type: General Medical Device

Manufacturer: GE Medical Systems Information Technologies, Inc.

Device ID: 150614

Wireless patient monitor/sensor reporting software, professional-onlyN/A

Type: General Medical Device

Manufacturer: GE Medical Systems Information Technologies, Inc.

Device ID: 150615

Orthopaedic fixation plate, non-bioabsorbable, non-sterileN/A

Type: General Medical Device

Manufacturer: Orthofix S.r.l.

Device ID: 78945

Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobialN/A

Type: General Medical Device

Manufacturer: Orthofix S.r.l.

Device ID: 127370

Orthopaedic implant aiming/guiding block, reusableN/A

Type: General Medical Device

Manufacturer: Orthofix S.r.l.

Device ID: 127346

Bone nail guidewire, reusableN/A

Type: General Medical Device

Manufacturer: Orthofix S.r.l.

Device ID: 101828

Other products from same authorized representative

Additional devices represented by UKCA Experts Ltd. in the UK

Nasal breathing aid, internal, reusableNov 26, 2024

Type: General Medical Device

Manufacturer: Airmax BV

Device ID: 169157

Dental/maxillofacial surgical procedure kit, non-medicated, reusableNov 26, 2024

Type: General Medical Device

Manufacturer: Cowellmedi

Device ID: 121889

Safe environment patient enclosureNov 26, 2024

Type: General Medical Device

Manufacturer: Human Protection B.V.

Device ID: 204049

Pliable-polymer dental regeneration membrane, bioabsorbable, tackedNov 26, 2024

Type: General Medical Device

Manufacturer: Cowellmedi

Device ID: 121892

Surgical/medical respirator, antimicrobialNov 26, 2024

Type: General Medical Device

Manufacturer: Profit Royal Pharmaceutical Limited

Device ID: 141563

Mental health/function therapeutic software, screen-viewedNov 26, 2024

Type: General Medical Device

Manufacturer: MindDoc Health GmbH

Device ID: 155595

Dental implant suprastructure, permanent, preformedNov 26, 2024

Type: General Medical Device

Manufacturer: Cowellmedi

Device ID: 121891

Screw endosteal dental implant, two-pieceNov 26, 2024

Type: General Medical Device

Manufacturer: Cowellmedi

Device ID: 121890

General-purpose multi-parameter bedside monitorNov 26, 2024

Type: General Medical Device

Manufacturer: SMARTCARDIA SA

Device ID: 154413

Breast implant delivery funnel, manualNov 26, 2024

Type: General Medical Device

Manufacturer: Kimsmed Co., Ltd.

Device ID: 121884

About this record

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 132011. The device is manufactured by DreamCon Co., Ltd. from South Korea, classified as General Medical Device. The authorized representative in the UK is UKCA Experts 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.

Free DatabasePowered by Pure Global AIMHRA RegisteredGeneral Medical Device