GUDIDData
eudamed_udi Primary ID: 03573026597320

CHROMID® Salmonella Elite (UDI 03573026597320)

Manufactured by bioMérieux SA

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CHROMID® Salmonella Elite - Primary ID 03573026597320

Device Regulatory Overview

The CHROMID® Salmonella Elite (Model/Catalog Number: 541928) is a medical device manufactured by bioMérieux SA. This product is indexed under FDA Product Code / Category Classification W0104010402 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
541928
Product Code / EMDN
W0104010402
Device Name
CHROMID® Salmonella Elite
Database Sync Date
2026-08-09 16:28:46

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 CHROMID® Salmonella Elite?

The registered manufacturer of record for CHROMID® Salmonella Elite is bioMérieux SA.

What is the Primary UDI-DI identifier for CHROMID® Salmonella Elite?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03573026597320.

What classification code is assigned to this device?

This device is registered under product classification code W0104010402.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint