eudamed_udi Primary ID: 08594072953804

PAN2.05 Ortéza klavikulární XL (UDI 08594072953804)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The PAN2.05 Ortéza klavikulární XL (Model/Catalog Number: PAN2.05 XL) is a medical device manufactured by PANOP CZ s.r.o.. This product is indexed under FDA Product Code / Category Classification Y060621 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: PAN2.05 XL
Product Code / EMDN: Y060621
Device Name: Ortéza klavikulární
Database Sync Date: 2026-08-09 16:50:16

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 PAN2.05 Ortéza klavikulární XL?

The registered manufacturer of record for PAN2.05 Ortéza klavikulární XL is PANOP CZ s.r.o..

What is the Primary UDI-DI identifier for PAN2.05 Ortéza klavikulární XL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594072953804.

What classification code is assigned to this device?

This device is registered under product classification code Y060621.

Similar Classification Devices (Y060621)

Other Devices by PANOP CZ s.r.o.

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