eudamed_udi Primary ID: 08594072953798

PAN2.05 Ortéza klavikulární L (UDI 08594072953798)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The PAN2.05 Ortéza klavikulární L (Model/Catalog Number: PAN2.05 L) 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 L
Product Code / EMDN: Y060621
Device Name: Ortéza klavikulární
Database Sync Date: 2026-08-09 16:51:36

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of PAN2.05 Ortéza klavikulární L?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594072953798.

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.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint