gudid
Primary ID: 9026561
CompoMat G5 Plus (UDI 9026561)
Manufactured by Fresenius Kabi AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CompoMat G5 Plus - Primary ID 9026561
Device Regulatory Overview
The CompoMat G5 Plus (Model/Catalog Number: 9026561) is a medical device manufactured by Fresenius Kabi AG. This product is indexed under FDA Product Code / Category Classification KSS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9026561
- Product Code / EMDN
- KSS
- Device Name
- The CompoMat G5/ CompoMat G5 Plus/ CompoMaster Net G5 Plus system is intended to be used as an automatic blood component separator for blood component separation and processing.
- Database Sync Date
- 2026-08-09 09:11:41
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 CompoMat G5 Plus?
The registered manufacturer of record for CompoMat G5 Plus is Fresenius Kabi AG.
What is the Primary UDI-DI identifier for CompoMat G5 Plus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9026561.
What classification code is assigned to this device?
This device is registered under product classification code KSS.
Similar Classification Devices (KSS)
Other Devices by Fresenius Kabi AG
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