eudamed_udi Primary ID: 08595626840038

PAN5.12 Ortéza zápěstí Manufix dlouhá M (UDI 08595626840038)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The PAN5.12 Ortéza zápěstí Manufix dlouhá M (Model/Catalog Number: PAN5.12 M) is a medical device manufactured by PANOP CZ s.r.o.. This product is indexed under FDA Product Code / Category Classification Y060609 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: PAN5.12 M
Product Code / EMDN: Y060609
Device Name: Ortéza zápěstí Manufix dlouhá
Database Sync Date: 2026-08-09 16:51:37

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 PAN5.12 Ortéza zápěstí Manufix dlouhá M?

The registered manufacturer of record for PAN5.12 Ortéza zápěstí Manufix dlouhá M is PANOP CZ s.r.o..

What is the Primary UDI-DI identifier for PAN5.12 Ortéza zápěstí Manufix dlouhá M?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08595626840038.

What classification code is assigned to this device?

This device is registered under product classification code Y060609.

Similar Classification Devices (Y060609)

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