GUDIDData
eudamed_udi Primary ID: 03760344760271

CHROMagar™ Campylobacter supplement (UDI 03760344760271)

Manufactured by CHROMagar™

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CHROMagar™ Campylobacter supplement - Primary ID 03760344760271

Device Regulatory Overview

The CHROMagar™ Campylobacter supplement (Model/Catalog Number: CP572(S)) 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
CP572(S)
Product Code / EMDN
W0104010104
Device Name
CHROMagar™ Campylobacter supplement
Database Sync Date
2026-08-09 16:50:32

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of CHROMagar™ Campylobacter supplement?

The registered manufacturer of record for CHROMagar™ Campylobacter supplement is CHROMagar™.

What is the Primary UDI-DI identifier for CHROMagar™ Campylobacter supplement?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760344760271.

What classification code is assigned to this device?

This device is registered under product classification code W0104010104.

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