eudamed_udi
Primary ID: 08437023168165
CINTURON DE SILLA (UDI 08437023168165)
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 CINTURON DE SILLA - Primary ID 08437023168165
Device Regulatory Overview
The CINTURON DE SILLA (Model/Catalog Number: 02101) is a medical device manufactured by EUROBASTON, S.L. - NIF B33851155. This product is indexed under FDA Product Code / Category Classification Y122403 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 02101
- Product Code / EMDN
- Y122403
- Device Name
- CINTURON DE SILLA
- Database Sync Date
- 2026-08-09 18:47:59
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of CINTURON DE SILLA?
The registered manufacturer of record for CINTURON DE SILLA is EUROBASTON, S.L. - NIF B33851155.
What is the Primary UDI-DI identifier for CINTURON DE SILLA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08437023168165.
What classification code is assigned to this device?
This device is registered under product classification code Y122403.
Similar Classification Devices (Y122403)
Other Devices by EUROBASTON, S.L. - NIF B33851155
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint