GUDIDData
eudamed_udi Primary ID: 08594072959196

PAN5.11 Ortéza zápěstí a palce ruky krátká M-levá (UDI 08594072959196)

Manufactured by PANOP CZ s.r.o.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PAN5.11 Ortéza zápěstí a palce ruky krátká M-levá - Primary ID 08594072959196

Device Regulatory Overview

The PAN5.11 Ortéza zápěstí a palce ruky krátká M-levá (Model/Catalog Number: PAN5.11 M-le) is a medical device manufactured by PANOP CZ s.r.o.. This product is indexed under FDA Product Code / Category Classification Y060612 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PAN5.11 M-le
Product Code / EMDN
Y060612
Device Name
Ortéza zápěstí a palce ruky krátká
Database Sync Date
2026-08-09 16:46:26

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 PAN5.11 Ortéza zápěstí a palce ruky krátká M-levá?

The registered manufacturer of record for PAN5.11 Ortéza zápěstí a palce ruky krátká M-levá is PANOP CZ s.r.o..

What is the Primary UDI-DI identifier for PAN5.11 Ortéza zápěstí a palce ruky krátká M-levá?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594072959196.

What classification code is assigned to this device?

This device is registered under product classification code Y060612.

Programmatic Export

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

JSON API Endpoint