eudamed_udi
Primary ID: 08431673412463
ALP (IFCC) (UDI 08431673412463)
Manufactured by Spinreact S.A.U.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ALP (IFCC) - Primary ID 08431673412463
Device Regulatory Overview
The ALP (IFCC) (Model/Catalog Number: 41246) is a medical device manufactured by Spinreact S.A.U.. This product is indexed under FDA Product Code / Category Classification W01010105 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 41246
- Product Code / EMDN
- W01010105
- Device Name
- Alkaline phosphatase
- Database Sync Date
- 2026-08-09 16:51:45
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 ALP (IFCC)?
The registered manufacturer of record for ALP (IFCC) is Spinreact S.A.U..
What is the Primary UDI-DI identifier for ALP (IFCC)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08431673412463.
What classification code is assigned to this device?
This device is registered under product classification code W01010105.
Similar Classification Devices (W01010105)
Other Devices by Spinreact S.A.U.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint