eudamed_udi
Primary ID: 03760344760134
CHROMagar™ STEC base (UDI 03760344760134)
Manufactured by CHROMagar™
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CHROMagar™ STEC base - Primary ID 03760344760134
Device Regulatory Overview
The CHROMagar™ STEC base (Model/Catalog Number: ST162(B)) is a medical device manufactured by CHROMagar™. This product is indexed under FDA Product Code / Category Classification W0104010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ST162(B)
- Product Code / EMDN
- W0104010101
- Device Name
- CHROMagar™ STEC base
- Database Sync Date
- 2026-08-09 18:00:47
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 CHROMagar™ STEC base?
The registered manufacturer of record for CHROMagar™ STEC base is CHROMagar™.
What is the Primary UDI-DI identifier for CHROMagar™ STEC base?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760344760134.
What classification code is assigned to this device?
This device is registered under product classification code W0104010101.
Similar Classification Devices (W0104010101)
Other Devices by CHROMagar™
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint