eudamed_udi Primary ID: 08594072959936

PAN8.11 Ortéza hlezna rigidní WALKAIR M (UDI 08594072959936)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The PAN8.11 Ortéza hlezna rigidní WALKAIR M (Model/Catalog Number: PAN8.11 M) is a medical device manufactured by PANOP CZ s.r.o.. This product is indexed under FDA Product Code / Category Classification Y06120601 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: PAN8.11 M
Product Code / EMDN: Y06120601
Device Name: Ortéza hlezna rigidní WALKAIR
Database Sync Date: 2026-08-09 16:29:24

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 PAN8.11 Ortéza hlezna rigidní WALKAIR M?

The registered manufacturer of record for PAN8.11 Ortéza hlezna rigidní WALKAIR M is PANOP CZ s.r.o..

What is the Primary UDI-DI identifier for PAN8.11 Ortéza hlezna rigidní WALKAIR M?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594072959936.

What classification code is assigned to this device?

This device is registered under product classification code Y06120601.

Similar Classification Devices (Y06120601)

Other Devices by PANOP CZ s.r.o.

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