eudamed_udi Primary ID: 08594072958533

PAN8.13 Bandáž hlezenní M (UDI 08594072958533)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The PAN8.13 Bandáž hlezenní M (Model/Catalog Number: PAN8.13 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: PAN8.13 M
Product Code / EMDN: Y06120601
Device Name: Bandáž hlezenní
Database Sync Date: 2026-08-09 16:51:32

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 PAN8.13 Bandáž hlezenní M?

The registered manufacturer of record for PAN8.13 Bandáž hlezenní M is PANOP CZ s.r.o..

What is the Primary UDI-DI identifier for PAN8.13 Bandáž hlezenní M?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594072958533.

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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