eudamed_udi Primary ID: 08594072953835

PAN3.01 Pás hrudní L (UDI 08594072953835)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The PAN3.01 Pás hrudní L (Model/Catalog Number: PAN3.01 L) is a medical device manufactured by PANOP CZ s.r.o.. This product is indexed under FDA Product Code / Category Classification M03040199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: PAN3.01 L
Product Code / EMDN: M03040199
Device Name: Pás hrudní
Database Sync Date: 2026-08-09 16:47:27

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 PAN3.01 Pás hrudní L?

The registered manufacturer of record for PAN3.01 Pás hrudní L is PANOP CZ s.r.o..

What is the Primary UDI-DI identifier for PAN3.01 Pás hrudní L?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594072953835.

What classification code is assigned to this device?

This device is registered under product classification code M03040199.

Similar Classification Devices (M03040199)

Other Devices by PANOP CZ s.r.o.

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