gudid Primary ID: Semiflex 3D, 0.07 cm ion chamber

NA (UDI Semiflex 3D, 0.07 cm ion chamber)

Manufactured by PTW-Freiburg Physikalisch-Technische Werksttten Dr. Pychlau GmbH

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

Scannable UDI-DI Representation

Device Regulatory Overview

The NA (Model/Catalog Number: Semiflex 3D, 0.07 cm ion chamber) is a medical device manufactured by PTW-Freiburg Physikalisch-Technische Werksttten Dr. Pychlau GmbH. This product is indexed under FDA Product Code / Category Classification LHN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Semiflex 3D, 0.07 cm ion chamber
Product Code / EMDN: LHN
Device Name
Database Sync Date: 2026-08-09 09:51:22

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 NA?

The registered manufacturer of record for NA is PTW-Freiburg Physikalisch-Technische Werksttten Dr. Pychlau GmbH.

What is the Primary UDI-DI identifier for NA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Semiflex 3D, 0.07 cm ion chamber.

What classification code is assigned to this device?

This device is registered under product classification code LHN.

Similar Classification Devices (LHN)

Other Devices by PTW-Freiburg Physikalisch-Technische Werksttten Dr. Pychlau GmbH

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