eudamed_udi
Primary ID: 08437023168349
Cojin coxis (UDI 08437023168349)
Manufactured by EUROBASTON, S.L. - NIF B33851155
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cojin coxis - Primary ID 08437023168349
Device Regulatory Overview
The Cojin coxis (Model/Catalog Number: 06211) is a medical device manufactured by EUROBASTON, S.L. - NIF B33851155. This product is indexed under FDA Product Code / Category Classification Y122406 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 06211
- Product Code / EMDN
- Y122406
- Device Name
- COJINES DE SILLA DE RUEDAS
- Database Sync Date
- 2026-08-09 17:34:35
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Cojin coxis?
The registered manufacturer of record for Cojin coxis is EUROBASTON, S.L. - NIF B33851155.
What is the Primary UDI-DI identifier for Cojin coxis?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08437023168349.
What classification code is assigned to this device?
This device is registered under product classification code Y122406.
Similar Classification Devices (Y122406)
Other Devices by EUROBASTON, S.L. - NIF B33851155
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