Liberty (UDI 026-20036A)
Manufactured by Fresenius Medical Care Holdings, Inc.
Device Regulatory Overview
The Liberty (Model/Catalog Number: 026-20036A) is a medical device manufactured by Fresenius Medical Care Holdings, Inc.. This product is indexed under FDA Product Code / Category Classification FKX within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- 026-20036A
- Product Code / EMDN
- FKX
- Device Name
- Liberty Drain Line
- Database Sync Date
- 2026-08-09 09:35:09
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 Liberty?
The registered manufacturer of record for Liberty is Fresenius Medical Care Holdings, Inc..
What is the Primary UDI-DI identifier for Liberty?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 026-20036A.
What classification code is assigned to this device?
This device is registered under product classification code FKX.
Similar Classification Devices (FKX)
Other Devices by Fresenius Medical Care Holdings, Inc.
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