GUDIDData
eudamed_udi Primary ID: 04250273728729

Back Check Valve (UDI 04250273728729)

Manufactured by Fresenius Kabi AG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Back Check Valve - Primary ID 04250273728729

Device Regulatory Overview

The Back Check Valve (Model/Catalog Number: 8502802) is a medical device manufactured by Fresenius Kabi AG. This product is indexed under FDA Product Code / Category Classification A0799 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
8502802
Product Code / EMDN
A0799
Device Name
Check Valves
Database Sync Date
2026-08-09 16:45:07

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 Back Check Valve?

The registered manufacturer of record for Back Check Valve is Fresenius Kabi AG.

What is the Primary UDI-DI identifier for Back Check Valve?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250273728729.

What classification code is assigned to this device?

This device is registered under product classification code A0799.

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