eudamed_udi Primary ID: 04250296160483

Erka. Switch Simplex (UDI 04250296160483)

Manufactured by ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Erka. Switch Simplex (Model/Catalog Number: 294.44894.7290) is a medical device manufactured by ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft. This product is indexed under FDA Product Code / Category Classification C9006 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 294.44894.7290
Product Code / EMDN: C9006
Device Name: Switch Simplex
Database Sync Date: 2026-08-09 16:29:24

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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Frequently Asked Questions

Who is the primary manufacturer of Erka. Switch Simplex?

The registered manufacturer of record for Erka. Switch Simplex is ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft.

What is the Primary UDI-DI identifier for Erka. Switch Simplex?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250296160483.

What classification code is assigned to this device?

This device is registered under product classification code C9006.

Similar Classification Devices (C9006)

Other Devices by ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft

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