eudamed_udi
Primary ID: 03760344760431
CHROMagar™ COL-APSE supplement (UDI 03760344760431)
Manufactured by CHROMagar™
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CHROMagar™ COL-APSE supplement - Primary ID 03760344760431
Device Regulatory Overview
The CHROMagar™ COL-APSE supplement (Model/Catalog Number: CO262(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
- CO262(S)
- Product Code / EMDN
- W0104010104
- Device Name
- CHROMagar™ COL-APSE supplement
- Database Sync Date
- 2026-08-09 16:29:15
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™ COL-APSE supplement?
The registered manufacturer of record for CHROMagar™ COL-APSE supplement is CHROMagar™.
What is the Primary UDI-DI identifier for CHROMagar™ COL-APSE supplement?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760344760431.
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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