gudid
Primary ID: N5C8305C
LOW RECIRCULATION VOLUME APD SET (UDI N5C8305C)
Manufactured by BAXTER INTERNATIONAL INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LOW RECIRCULATION VOLUME APD SET - Primary ID N5C8305C
Device Regulatory Overview
The LOW RECIRCULATION VOLUME APD SET (Model/Catalog Number: N5C8305C) is a medical device manufactured by BAXTER INTERNATIONAL INC.. This product is indexed under FDA Product Code / Category Classification FKX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- N5C8305C
- Product Code / EMDN
- FKX
- Device Name
- This automated PD Set is compatible with Baxter Automated PD systems, Baxter PD Transfer Sets and Effluent Sample Bag. Low Recirculation Volume APD set with cassette
- 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 LOW RECIRCULATION VOLUME APD SET?
The registered manufacturer of record for LOW RECIRCULATION VOLUME APD SET is BAXTER INTERNATIONAL INC..
What is the Primary UDI-DI identifier for LOW RECIRCULATION VOLUME APD SET?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is N5C8305C.
What classification code is assigned to this device?
This device is registered under product classification code FKX.
Similar Classification Devices (FKX)
Other Devices by BAXTER INTERNATIONAL INC.
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