GUDIDData
eudamed_udi Primary ID: 04260586041842

Einmalbehältersystem (inkl. “Bag“ und “OneWay“) (UDI 04260586041842)

Manufactured by ASSKEA GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Einmalbehältersystem (inkl. “Bag“ und “OneWay“) - Primary ID 04260586041842

Device Regulatory Overview

The Einmalbehältersystem (inkl. “Bag“ und “OneWay“) (Model/Catalog Number: 67714) is a medical device manufactured by ASSKEA GmbH. This product is indexed under FDA Product Code / Category Classification A060399 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
67714
Product Code / EMDN
A060399
Device Name
Behandlungseinheit Zubehör
Database Sync Date
2026-08-09 18:02:39

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 Einmalbehältersystem (inkl. “Bag“ und “OneWay“)?

The registered manufacturer of record for Einmalbehältersystem (inkl. “Bag“ und “OneWay“) is ASSKEA GmbH.

What is the Primary UDI-DI identifier for Einmalbehältersystem (inkl. “Bag“ und “OneWay“)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260586041842.

What classification code is assigned to this device?

This device is registered under product classification code A060399.

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