eudamed_udi Primary ID: 08594072957000

PAN3.05 Pás bederní s výztuhami S (UDI 08594072957000)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The PAN3.05 Pás bederní s výztuhami S (Model/Catalog Number: PAN3.05 S) is a medical device manufactured by PANOP CZ s.r.o.. This product is indexed under FDA Product Code / Category Classification Y060306 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: PAN3.05 S
Product Code / EMDN: Y060306
Device Name: Pás bederní s výztuhami
Database Sync Date: 2026-08-09 16:51:39

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 PAN3.05 Pás bederní s výztuhami S?

The registered manufacturer of record for PAN3.05 Pás bederní s výztuhami S is PANOP CZ s.r.o..

What is the Primary UDI-DI identifier for PAN3.05 Pás bederní s výztuhami S?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594072957000.

What classification code is assigned to this device?

This device is registered under product classification code Y060306.

Similar Classification Devices (Y060306)

Other Devices by PANOP CZ s.r.o.

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