gudid Primary ID: Dosimetry Diode PR

NA (UDI Dosimetry Diode PR)

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: Dosimetry Diode PR) is a medical device manufactured by PTW-Freiburg Physikalisch-Technische Werksttten Dr. Pychlau GmbH. This product is indexed under FDA Product Code / Category Classification IYE within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Dosimetry Diode PR
Product Code / EMDN: IYE
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 Dosimetry Diode PR.

What classification code is assigned to this device?

This device is registered under product classification code IYE.

Similar Classification Devices (IYE)

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

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