GUDIDData
eudamed_udi Primary ID: 08594072954931

PAN7.08 Ortéza krátká kolenní s limitací L (UDI 08594072954931)

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 PAN7.08 Ortéza krátká kolenní s limitací L - Primary ID 08594072954931

Device Regulatory Overview

The PAN7.08 Ortéza krátká kolenní s limitací L (Model/Catalog Number: PAN7.08 L) 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
PAN7.08 L
Product Code / EMDN
Y061209
Device Name
Ortéza krátká kolenní s limitací
Database Sync Date
2026-08-09 16:47:26

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 PAN7.08 Ortéza krátká kolenní s limitací L?

The registered manufacturer of record for PAN7.08 Ortéza krátká kolenní s limitací L is PANOP CZ s.r.o..

What is the Primary UDI-DI identifier for PAN7.08 Ortéza krátká kolenní s limitací L?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594072954931.

What classification code is assigned to this device?

This device is registered under product classification code Y061209.

Programmatic Export

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

JSON API Endpoint