eudamed_udi Primary ID: 08594072955204

PAN5.01 Ortéza zápěstí krátká XL-levá (UDI 08594072955204)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The PAN5.01 Ortéza zápěstí krátká XL-levá (Model/Catalog Number: PAN5.01 XL-le) is a medical device manufactured by PANOP CZ s.r.o.. This product is indexed under FDA Product Code / Category Classification Y060609 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: PAN5.01 XL-le
Product Code / EMDN: Y060609
Device Name: Ortéza zápěstí krátká
Database Sync Date: 2026-08-09 16:50:46

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 PAN5.01 Ortéza zápěstí krátká XL-levá?

The registered manufacturer of record for PAN5.01 Ortéza zápěstí krátká XL-levá is PANOP CZ s.r.o..

What is the Primary UDI-DI identifier for PAN5.01 Ortéza zápěstí krátká XL-levá?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594072955204.

What classification code is assigned to this device?

This device is registered under product classification code Y060609.

Similar Classification Devices (Y060609)

Other Devices by PANOP CZ s.r.o.

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