eudamed_udi Primary ID: 08594072959288

PAN7.13 Ortéza kolenní s křížovým tahem XL (UDI 08594072959288)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The PAN7.13 Ortéza kolenní s křížovým tahem XL (Model/Catalog Number: PAN7.13 XL) is a medical device manufactured by PANOP CZ s.r.o.. This product is indexed under FDA Product Code / Category Classification Y061209 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: PAN7.13 XL
Product Code / EMDN: Y061209
Device Name: Ortéza kolenní s křížovým tahem
Database Sync Date: 2026-08-09 16:51:34

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 PAN7.13 Ortéza kolenní s křížovým tahem XL?

The registered manufacturer of record for PAN7.13 Ortéza kolenní s křížovým tahem XL is PANOP CZ s.r.o..

What is the Primary UDI-DI identifier for PAN7.13 Ortéza kolenní s křížovým tahem XL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594072959288.

What classification code is assigned to this device?

This device is registered under product classification code Y061209.

Similar Classification Devices (Y061209)

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