eudamed_udi Primary ID: 08594072954863

PAN4.02 Ortéza lokte s limitací XXS (UDI 08594072954863)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The PAN4.02 Ortéza lokte s limitací XXS (Model/Catalog Number: PAN4.02 XXS) is a medical device manufactured by PANOP CZ s.r.o.. This product is indexed under FDA Product Code / Category Classification Y060615 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: PAN4.02 XXS
Product Code / EMDN: Y060615
Device Name: Ortéza lokte s limitací
Database Sync Date: 2026-08-09 16:46:59

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 PAN4.02 Ortéza lokte s limitací XXS?

The registered manufacturer of record for PAN4.02 Ortéza lokte s limitací XXS is PANOP CZ s.r.o..

What is the Primary UDI-DI identifier for PAN4.02 Ortéza lokte s limitací XXS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594072954863.

What classification code is assigned to this device?

This device is registered under product classification code Y060615.

Similar Classification Devices (Y060615)

Other Devices by PANOP CZ s.r.o.

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