gudid Primary ID: H154-11314

Hermann Medizintechnik GmbH (UDI H154-11314)

Manufactured by Hermann Medizintechnik GmbH

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Hermann Medizintechnik GmbH (Model/Catalog Number: H154-11314) is a medical device manufactured by Hermann Medizintechnik GmbH. This product is indexed under FDA Product Code / Category Classification KCF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: H154-11314
Product Code / EMDN: KCF
Device Name: LABORDE tracheal dilator, length 14cm
Database Sync Date: 2026-08-09 09:11:47

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 Hermann Medizintechnik GmbH?

The registered manufacturer of record for Hermann Medizintechnik GmbH is Hermann Medizintechnik GmbH.

What is the Primary UDI-DI identifier for Hermann Medizintechnik GmbH?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is H154-11314.

What classification code is assigned to this device?

This device is registered under product classification code KCF.

Similar Classification Devices (KCF)

Other Devices by Hermann Medizintechnik GmbH

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