gudid
Primary ID: 2C6921
INTERLINK (UDI 2C6921)
Manufactured by BAXTER INTERNATIONAL INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for INTERLINK - Primary ID 2C6921
Device Regulatory Overview
The INTERLINK (Model/Catalog Number: 2C6921) is a medical device manufactured by BAXTER INTERNATIONAL INC.. This product is indexed under FDA Product Code / Category Classification FMG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2C6921
- Product Code / EMDN
- FMG
- Device Name
- 3-Port Manifold with Check Valves, Large Bore Stopcock with Rotating Male Luer Lock Extension Set, 2 Injection Sites, 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 INTERLINK?
The registered manufacturer of record for INTERLINK is BAXTER INTERNATIONAL INC..
What is the Primary UDI-DI identifier for INTERLINK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2C6921.
What classification code is assigned to this device?
This device is registered under product classification code FMG.
Similar Classification Devices (FMG)
Other Devices by BAXTER INTERNATIONAL INC.
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