GUDIDData
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enforcement Primary ID: Z-0745-2016

DS/US Proton Feature with Pinnacle3 Software Version 10.0.0 and 14.0.0 Radiation Therapy Planning System Model #459800200621 (UDI Z-0745-2016)

Manufactured by Philips Medical Systems

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DS/US Proton Feature with Pinnacle3 Software Version 10.0.0 and 14.0.0 Radiation Therapy Planning System Model #459800200621 - Primary ID Z-0745-2016

Device Regulatory Overview

The DS/US Proton Feature with Pinnacle3 Software Version 10.0.0 and 14.0.0 Radiation Therapy Planning System Model #459800200621 (Model/Catalog Number: Unspecified) is a medical device manufactured by Philips Medical Systems. This product is indexed under FDA Product Code / Category Classification Software Version 10.0.0 and 14.0.0 within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

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Technical Specifications

Model Number
N/A
Device Name
DS/US Proton Feature with Pinnacle3 Software Version 10.0.0 and 14.0.0 Radiation Therapy Planning System Model #459800200621
Database Sync Date
2026-08-09 10:06:44

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 DS/US Proton Feature with Pinnacle3 Software Version 10.0.0 and 14.0.0 Radiation Therapy Planning System Model #459800200621?

The registered manufacturer of record for DS/US Proton Feature with Pinnacle3 Software Version 10.0.0 and 14.0.0 Radiation Therapy Planning System Model #459800200621 is Philips Medical Systems.

What is the Primary UDI-DI identifier for DS/US Proton Feature with Pinnacle3 Software Version 10.0.0 and 14.0.0 Radiation Therapy Planning System Model #459800200621?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Z-0745-2016.

What classification code is assigned to this device?

This device is registered under product classification code Software Version 10.0.0 and 14.0.0.

Other Devices by Philips Medical Systems

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