gudid
Primary ID: 6N8399
V-LINK/VITALSHIELD (UDI 6N8399)
Manufactured by BAXTER INTERNATIONAL INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for V-LINK/VITALSHIELD - Primary ID 6N8399
Device Regulatory Overview
The V-LINK/VITALSHIELD (Model/Catalog Number: 6N8399) 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
- 6N8399
- Product Code / EMDN
- FPA
- Device Name
- V-LINK, Luer Activated Device with VITALSHIELD Protective Coating
- 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
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of V-LINK/VITALSHIELD?
The registered manufacturer of record for V-LINK/VITALSHIELD is BAXTER INTERNATIONAL INC..
What is the Primary UDI-DI identifier for V-LINK/VITALSHIELD?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6N8399.
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.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint