eudamed_udi Primary ID: 08595626810215

PAN4.06 Bandáž loketní XXS (UDI 08595626810215)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The PAN4.06 Bandáž loketní XXS (Model/Catalog Number: PAN4.06 XXS) 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: PAN4.06 XXS
Product Code / EMDN: M030299
Device Name: Bandáž loketní
Database Sync Date: 2026-08-09 17:27:33

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 PAN4.06 Bandáž loketní XXS?

The registered manufacturer of record for PAN4.06 Bandáž loketní XXS is PANOP CZ s.r.o..

What is the Primary UDI-DI identifier for PAN4.06 Bandáž loketní XXS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08595626810215.

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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