gudid
Primary ID: 9025561
CompoMat G5 (UDI 9025561)
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 - Primary ID 9025561
Device Regulatory Overview
The CompoMat G5 (Model/Catalog Number: 9025561) 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
- 9025561
- Product Code / EMDN
- KSS
- Device Name
- The CompoMat G5 / CompoMaster Net G5 System is intended as an automated blood component separator used for blood component separation and preparation.The CompoMat G5 can carry out almost all preparation methods and handle almost all blood bag systems, such as conventional double, triple and quadruple blood bag systems.
- 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?
The registered manufacturer of record for CompoMat G5 is Fresenius Kabi AG.
What is the Primary UDI-DI identifier for CompoMat G5?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9025561.
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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