gudid
Primary ID: 2N8341
CLEARLINK (UDI 2N8341)
Manufactured by BAXTER INTERNATIONAL INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CLEARLINK - Primary ID 2N8341
Device Regulatory Overview
The CLEARLINK (Model/Catalog Number: 2N8341) 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
- 2N8341
- Product Code / EMDN
- FPA
- Device Name
- Non-DEHP Three Lead Extension Set, Luer Activated Valve for I.V. Access, 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 CLEARLINK?
The registered manufacturer of record for CLEARLINK is BAXTER INTERNATIONAL INC..
What is the Primary UDI-DI identifier for CLEARLINK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2N8341.
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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