GUDIDData
gudid Primary ID: 2H8454

CLEARLINK/CONTINU-FLO (UDI 2H8454)

Manufactured by BAXTER HEALTHCARE CORPORATION

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CLEARLINK/CONTINU-FLO - Primary ID 2H8454

Device Regulatory Overview

The CLEARLINK/CONTINU-FLO (Model/Catalog Number: 2H8454) is a medical device manufactured by BAXTER HEALTHCARE CORPORATION. This product is indexed under FDA Product Code / Category Classification FMG within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 2 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-2174-2021 View Full Alert →

Kaguya Automated Peritoneal Dialysis System...

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ID: Z-2173-2021 View Full Alert →

Sharesource Connectivity Platform for Use with the Amia Automated PD System...

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Technical Specifications

Model Number
2H8454
Product Code / EMDN
FMG
Device Name
Non-DEHP CONTINU-FLO Solution Set, 2 Luer Activated Valves, Male Luer Lock Adapter with Retractable Collar, Non-DEHP Large Bore Stopcock Extension Set, Large Bore Stopcock Manifold, Luer Activated Valve, Male Luer Lock Adapter with Retractable Collar
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
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of CLEARLINK/CONTINU-FLO?

The registered manufacturer of record for CLEARLINK/CONTINU-FLO is BAXTER HEALTHCARE CORPORATION.

What is the Primary UDI-DI identifier for CLEARLINK/CONTINU-FLO?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2H8454.

What classification code is assigned to this device?

This device is registered under product classification code FMG.

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