eudamed_udi Primary ID: 08594072954306

PAN7.02 Ortéza kolenního kloubu přímá M (UDI 08594072954306)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The PAN7.02 Ortéza kolenního kloubu přímá M (Model/Catalog Number: PAN7.02 M) 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: PAN7.02 M
Product Code / EMDN: Y061209
Device Name: Ortéza kolenního kloubu přímá
Database Sync Date: 2026-08-09 16:46:54

Full Regulatory Attributes

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

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Frequently Asked Questions

Who is the primary manufacturer of PAN7.02 Ortéza kolenního kloubu přímá M?

The registered manufacturer of record for PAN7.02 Ortéza kolenního kloubu přímá M is PANOP CZ s.r.o..

What is the Primary UDI-DI identifier for PAN7.02 Ortéza kolenního kloubu přímá M?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594072954306.

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.

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