gudid
Primary ID: XPH170
Xenium XPH Dialyzer (UDI XPH170)
Manufactured by BAXTER INTERNATIONAL INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Xenium XPH Dialyzer - Primary ID XPH170
Device Regulatory Overview
The Xenium XPH Dialyzer (Model/Catalog Number: XPH170) is a medical device manufactured by BAXTER INTERNATIONAL INC.. This product is indexed under FDA Product Code / Category Classification KDI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- XPH170
- Product Code / EMDN
- KDI
- Device Name
- Hemodialysis with XENIUM XPH Dialyzer is indicated for patients with acute or chronic renal failure when conservative therapy is judged to be inadequate. It also may be indicated in the treatment of patients intoxicated with poisons or drugs.
- Database Sync Date
- 2026-08-09 09:08:43
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 Xenium XPH Dialyzer?
The registered manufacturer of record for Xenium XPH Dialyzer is BAXTER INTERNATIONAL INC..
What is the Primary UDI-DI identifier for Xenium XPH Dialyzer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is XPH170.
What classification code is assigned to this device?
This device is registered under product classification code KDI.
Similar Classification Devices (KDI)
Other Devices by BAXTER INTERNATIONAL INC.
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