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Rider - EUDAMED Registration 05060639240760

Access comprehensive regulatory information for Rider in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI 05060639240760 and manufactured by Open Bionics Ltd. in United Kingdom (ex Northern Ireland).

This page provides complete registration details including trade name (Rider), manufacturer information, authorized representative details, competent authority (Health Products Regulatory Authority, Medical Devices Department), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.

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EUDAMED Official Data
Class I
05060639240760
No
Rider
Trade Name: Rider
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Device Description (EMDN)

UPPER LIMB ORTHOSES - ACCESSORIES

Device Classification
Risk Class
Class I
CND Nomenclatures Code
Y060680
Trade Name
Rider
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
05060639240760
Basic UDI
506063924RiderPS
Version Date
February 05, 2025
Manufacturer Last Update
January 13, 2023
Active Status
No
Manufacturer
Manufacturer Name
Open Bionics Ltd.
Country
United Kingdom (ex Northern Ireland)
Country Type
NON_EU
Address
Programme Tower Lane Bristol
Email
hello@openbionics.com
Authorized Representative
SRN
IE-AR-000003999
Country
Ireland
Address
Stratton House, BISHOPSTOWN ROAD CORK
Email
tqmuk@aol.com
Telephone
+447545595464
Regulatory Information
Competent Authority
Health Products Regulatory Authority, Medical Devices Department
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
Germany
Device Characteristics
Human Tissues
No
Animal Tissues
No