eudamed_udi
Primary ID: 03760344760202
CHROMagar™ ESBL supplement (UDI 03760344760202)
Manufactured by CHROMagar™
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CHROMagar™ ESBL supplement - Primary ID 03760344760202
Device Regulatory Overview
The CHROMagar™ ESBL supplement (Model/Catalog Number: ES372) is a medical device manufactured by CHROMagar™. This product is indexed under FDA Product Code / Category Classification W0104010104 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ES372
- Product Code / EMDN
- W0104010104
- Device Name
- CHROMagar™ ESBL supplement
- Database Sync Date
- 2026-08-09 18:03:34
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™ ESBL supplement?
The registered manufacturer of record for CHROMagar™ ESBL supplement is CHROMagar™.
What is the Primary UDI-DI identifier for CHROMagar™ ESBL supplement?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760344760202.
What classification code is assigned to this device?
This device is registered under product classification code W0104010104.
Similar Classification Devices (W0104010104)
Other Devices by CHROMagar™
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint