GUDIDData
eudamed_udi Primary ID: 08594072959134

PAN5.10 Ortéza zápěstí fixační s oporou pod prsty L-pravá (UDI 08594072959134)

Manufactured by PANOP CZ s.r.o.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PAN5.10 Ortéza zápěstí fixační s oporou pod prsty L-pravá - Primary ID 08594072959134

Device Regulatory Overview

The PAN5.10 Ortéza zápěstí fixační s oporou pod prsty L-pravá (Model/Catalog Number: PAN5.10 L-pr) is a medical device manufactured by PANOP CZ s.r.o.. This product is indexed under FDA Product Code / Category Classification Y060613 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PAN5.10 L-pr
Product Code / EMDN
Y060613
Device Name
Ortéza zápěstí fixační s oporou pod prsty
Database Sync Date
2026-08-09 16:45:40

Full Regulatory Attributes

🔒 Token Gated
{
    "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 PAN5.10 Ortéza zápěstí fixační s oporou pod prsty L-pravá?

The registered manufacturer of record for PAN5.10 Ortéza zápěstí fixační s oporou pod prsty L-pravá is PANOP CZ s.r.o..

What is the Primary UDI-DI identifier for PAN5.10 Ortéza zápěstí fixační s oporou pod prsty L-pravá?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594072959134.

What classification code is assigned to this device?

This device is registered under product classification code Y060613.

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