Dental prosthesis veneer resin - UK MHRA Medical Device Registration

Dental prosthesis veneer resin is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 76820. The device is manufactured by DIO Corporation from South Korea, classified as General Medical Device. The authorized representative in the UK is Compliance Solutions (Lifesciences) 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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Dental prosthesis veneer resin

MHRA Device ID: 76820•Ref: 76820

Device Type

General Medical Device

Devices

Dental prosthesis veneer resin

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jan 16, 2024

Manufacturer Information

Name

DIO Corporation

Address

66, Centumseo-ro Haeundae-gu

Busan, South Korea

Created Date

Mar 22, 2021

Authorized Representative

Name

Compliance Solutions (Lifesciences) Ltd

Relationship Type

UK Responsible Person

Address

Suite 10, Dunswood House 1 Dunswood Road Cumbernauld

Glasgow, United Kingdom

Postcode: G67 3EN

DJ Fang

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Other Products from DIO Corporation (10)

Other Products from Same Authorized Representative (10)

Dental prosthesis veneer resin - 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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