eudamed_udi Primary ID: 08594072956508

PAN4.04 Bandáž lokte s epipáskou XL (UDI 08594072956508)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The PAN4.04 Bandáž lokte s epipáskou XL (Model/Catalog Number: PAN4.04 XL) is a medical device manufactured by PANOP CZ s.r.o.. This product is indexed under FDA Product Code / Category Classification M030299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: PAN4.04 XL
Product Code / EMDN: M030299
Device Name: Bandáž lokte s epipáskou
Database Sync Date: 2026-08-09 18:24:55

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 PAN4.04 Bandáž lokte s epipáskou XL?

The registered manufacturer of record for PAN4.04 Bandáž lokte s epipáskou XL is PANOP CZ s.r.o..

What is the Primary UDI-DI identifier for PAN4.04 Bandáž lokte s epipáskou XL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594072956508.

What classification code is assigned to this device?

This device is registered under product classification code M030299.

Similar Classification Devices (M030299)

Other Devices by PANOP CZ s.r.o.

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