eudamed_udi
Primary ID: 05904708000513
Columbia Agar + 5% Sheep Blood (UDI 05904708000513)
Manufactured by GRASO Zenon Sobiecki
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Columbia Agar + 5% Sheep Blood - Primary ID 05904708000513
Device Regulatory Overview
The Columbia Agar + 5% Sheep Blood (Model/Catalog Number: 1190PD140) is a medical device manufactured by GRASO Zenon Sobiecki. This product is indexed under FDA Product Code / Category Classification W0104010405 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1190PD140
- Product Code / EMDN
- W0104010405
- Device Name
- Columbia Agar + 5% Sheep Blood
- Database Sync Date
- 2026-08-09 16:28:58
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 Columbia Agar + 5% Sheep Blood?
The registered manufacturer of record for Columbia Agar + 5% Sheep Blood is GRASO Zenon Sobiecki.
What is the Primary UDI-DI identifier for Columbia Agar + 5% Sheep Blood?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05904708000513.
What classification code is assigned to this device?
This device is registered under product classification code W0104010405.
Similar Classification Devices (W0104010405)
Other Devices by GRASO Zenon Sobiecki
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint