gudid
Primary ID: R5C4479
NA (UDI R5C4479)
Manufactured by Baxter Healthcare SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NA - Primary ID R5C4479
Device Regulatory Overview
The NA (Model/Catalog Number: R5C4479) is a medical device manufactured by Baxter Healthcare SA. This product is indexed under FDA Product Code / Category Classification FKX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- R5C4479
- Product Code / EMDN
- FKX
- Device Name
- HomeChoice Automated PD Set with Cassette and 4-Prong Luers
- 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 NA?
The registered manufacturer of record for NA is Baxter Healthcare SA.
What is the Primary UDI-DI identifier for NA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is R5C4479.
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 Healthcare SA
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