CHROMagarTM Acinetobacter MDR Agar (UDI 84365422215046)
Manufactured by Reactivos para Diagnóstico
Device Regulatory Overview
The CHROMagarTM Acinetobacter MDR Agar (Model/Catalog Number: PA6201) is a medical device manufactured by Reactivos para Diagnóstico. This product is indexed under FDA Product Code / Category Classification W0104010404 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PA6201
- Product Code / EMDN
- W0104010404
- Device Name
- CHROMagar ™ Acinetobacter Agar
- Database Sync Date
- 2026-08-09 19:05:21
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 CHROMagarTM Acinetobacter MDR Agar?
The registered manufacturer of record for CHROMagarTM Acinetobacter MDR Agar is Reactivos para Diagnóstico.
What is the Primary UDI-DI identifier for CHROMagarTM Acinetobacter MDR Agar?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 84365422215046.
What classification code is assigned to this device?
This device is registered under product classification code W0104010404.
Similar Classification Devices (W0104010404)
Other Devices by Reactivos para Diagnóstico
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint