gudid
Primary ID: 2H7452
INTERLINK/DUO-VENT (UDI 2H7452)
Manufactured by BAXTER INTERNATIONAL INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for INTERLINK/DUO-VENT - Primary ID 2H7452
Device Regulatory Overview
The INTERLINK/DUO-VENT (Model/Catalog Number: 2H7452) 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
- 2H7452
- Product Code / EMDN
- FPA
- Device Name
- Non-DEHP Secondary Medication Set with DUO-VENT Spike, Hanger, Lever Lock Cannula, Male Luer Lock Adapter
- 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 INTERLINK/DUO-VENT?
The registered manufacturer of record for INTERLINK/DUO-VENT is BAXTER INTERNATIONAL INC..
What is the Primary UDI-DI identifier for INTERLINK/DUO-VENT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2H7452.
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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