eudamed_udi
Primary ID: 50604724675152
Unspecified Brand (UDI 50604724675152)
Manufactured by Pro-Lab Diagnostics UK
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 50604724675152
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: PL.850-3) is a medical device manufactured by Pro-Lab Diagnostics UK. This product is indexed under FDA Product Code / Category Classification W0105011203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PL.850-3
- Product Code / EMDN
- W0105011203
- Device Name
- Rabbit Coagulase Plasma 10 x 3.0ml
- Database Sync Date
- 2026-08-09 17:25:50
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Pro-Lab Diagnostics UK.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 50604724675152.
What classification code is assigned to this device?
This device is registered under product classification code W0105011203.
Similar Classification Devices (W0105011203)
Other Devices by Pro-Lab Diagnostics UK
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint