GUDIDData
eudamed_udi Primary ID: 08594072954351

PAN7.03 Ortéza kolenního kloubu s flexí 20st L (UDI 08594072954351)

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 PAN7.03 Ortéza kolenního kloubu s flexí 20st L - Primary ID 08594072954351

Device Regulatory Overview

The PAN7.03 Ortéza kolenního kloubu s flexí 20st L (Model/Catalog Number: PAN7.03 L) is a medical device manufactured by PANOP CZ s.r.o.. This product is indexed under FDA Product Code / Category Classification Y061209 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PAN7.03 L
Product Code / EMDN
Y061209
Device Name
Ortéza kolenního kloubu s flexí 20st
Database Sync Date
2026-08-09 16:29:32

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 PAN7.03 Ortéza kolenního kloubu s flexí 20st L?

The registered manufacturer of record for PAN7.03 Ortéza kolenního kloubu s flexí 20st L is PANOP CZ s.r.o..

What is the Primary UDI-DI identifier for PAN7.03 Ortéza kolenního kloubu s flexí 20st L?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594072954351.

What classification code is assigned to this device?

This device is registered under product classification code Y061209.

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