eudamed_udi
Primary ID: 03760344760226
CHROMagar™ Orientation (UDI 03760344760226)
Manufactured by CHROMagar™
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CHROMagar™ Orientation - Primary ID 03760344760226
Device Regulatory Overview
The CHROMagar™ Orientation (Model/Catalog Number: RT413-25) is a medical device manufactured by CHROMagar™. This product is indexed under FDA Product Code / Category Classification W0104010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RT413-25
- Product Code / EMDN
- W0104010101
- Device Name
- CHROMagar™ Orientation
- Database Sync Date
- 2026-08-09 17:56:10
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™ Orientation?
The registered manufacturer of record for CHROMagar™ Orientation is CHROMagar™.
What is the Primary UDI-DI identifier for CHROMagar™ Orientation?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760344760226.
What classification code is assigned to this device?
This device is registered under product classification code W0104010101.
Similar Classification Devices (W0104010101)
Other Devices by CHROMagar™
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