eudamed_udi
Primary ID: 03760344760059
CHROMagar™ Acinetobacter supplement (UDI 03760344760059)
Manufactured by CHROMagar™
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CHROMagar™ Acinetobacter supplement - Primary ID 03760344760059
Device Regulatory Overview
The CHROMagar™ Acinetobacter supplement (Model/Catalog Number: AC092(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
- AC092(S)
- Product Code / EMDN
- W0104010104
- Device Name
- CHROMagar™ Acinetobacter supplement
- Database Sync Date
- 2026-08-09 18:13:34
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of CHROMagar™ Acinetobacter supplement?
The registered manufacturer of record for CHROMagar™ Acinetobacter supplement is CHROMagar™.
What is the Primary UDI-DI identifier for CHROMagar™ Acinetobacter supplement?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760344760059.
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™
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