Spectacle frame - UK MHRA Medical Device Registration

Spectacle frame is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 152003. The device is manufactured by Rudy Project S.p.A. from Italy, classified as General Medical Device. The authorized representative in the UK is Donawa Lifescience 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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Spectacle frame

MHRA Device ID: 152003•Ref: 152003

Device Type

General Medical Device

Devices

Spectacle frame

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Oct 7, 2023

Manufacturer Information

Name

Rudy Project S.p.A.

Address

Via B. Marcello 44

Treviso, TV, Italy

Created Date

Jul 14, 2022

Authorized Representative

Name

Donawa Lifescience Ltd

Relationship Type

UK Responsible Person

Address

Aviation Business Park Enterprise Close

Christchurch, England, United Kingdom

Postcode: BH23 6NX

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Other Products from Rudy Project S.p.A. (1)

Prescription spectacle lens, custom-made

Type: General Medical Device

Registered: Nov 26, 2024

Other Products from Same Authorized Representative (10)

Spectacle frame - UK MHRA Medical Device Registration

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