eudamed_udi
Primary ID: 08435491810388
FÉRULA DE STACK ; STACK SPLINTS (UDI 08435491810388)
Manufactured by Orliman, S.L.U.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FÉRULA DE STACK ; STACK SPLINTS - Primary ID 08435491810388
Device Regulatory Overview
The FÉRULA DE STACK ; STACK SPLINTS (Model/Catalog Number: ACV501#6) is a medical device manufactured by Orliman, S.L.U.. This product is indexed under FDA Product Code / Category Classification Y060603 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ACV501#6
- Product Code / EMDN
- Y060603
- Device Name
- Férulas dedo
- Database Sync Date
- 2026-08-09 16:29:55
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 FÉRULA DE STACK ; STACK SPLINTS?
The registered manufacturer of record for FÉRULA DE STACK ; STACK SPLINTS is Orliman, S.L.U..
What is the Primary UDI-DI identifier for FÉRULA DE STACK ; STACK SPLINTS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435491810388.
What classification code is assigned to this device?
This device is registered under product classification code Y060603.
Similar Classification Devices (Y060603)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint