gudid
Primary ID: 2N1333
NA (UDI 2N1333)
Manufactured by BAXTER INTERNATIONAL INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NA - Primary ID 2N1333
Device Regulatory Overview
The NA (Model/Catalog Number: 2N1333) is a medical device manufactured by BAXTER INTERNATIONAL INC.. This product is indexed under FDA Product Code / Category Classification FPA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2N1333
- Product Code / EMDN
- FPA
- Device Name
- Non-DEHP Standard Bore Catheter Extension Set, Power Injectable, Male Luer Lock Adapter with Retractable Collar
- 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 INTERNATIONAL INC..
What is the Primary UDI-DI identifier for NA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2N1333.
What classification code is assigned to this device?
This device is registered under product classification code FPA.
Similar Classification Devices (FPA)
Other Devices by BAXTER INTERNATIONAL INC.
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