Espaciador de rodilla SUBITON EVOLUTION (UDI 07798034468677)
Manufactured by Laboratorios SL S.A.
Device Regulatory Overview
The Espaciador de rodilla SUBITON EVOLUTION (Model/Catalog Number: 880867) is a medical device manufactured by Laboratorios SL S.A.. This product is indexed under FDA Product Code / Category Classification P090908 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 880867
- Product Code / EMDN
- P090908
- Device Name
- Espaciador de rodilla con gentamicina
- Database Sync Date
- 2026-08-09 16:51:23
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 Espaciador de rodilla SUBITON EVOLUTION?
The registered manufacturer of record for Espaciador de rodilla SUBITON EVOLUTION is Laboratorios SL S.A..
What is the Primary UDI-DI identifier for Espaciador de rodilla SUBITON EVOLUTION?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07798034468677.
What classification code is assigned to this device?
This device is registered under product classification code P090908.
Similar Classification Devices (P090908)
Other Devices by Laboratorios SL S.A.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint