gudid
Primary ID: 150
Exeltra Dialyzer (UDI 150)
Manufactured by BAXTER INTERNATIONAL INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Exeltra Dialyzer - Primary ID 150
Device Regulatory Overview
The Exeltra Dialyzer (Model/Catalog Number: 150) 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
- 150
- Product Code / EMDN
- KDI
- Device Name
- Hemodialysis with EXELTRA and EXELTRA Plus dialyzers 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
🔒 Token Gated
{
"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 Exeltra Dialyzer?
The registered manufacturer of record for Exeltra Dialyzer is BAXTER INTERNATIONAL INC..
What is the Primary UDI-DI identifier for Exeltra Dialyzer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 150.
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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