GUDIDData
eudamed_udi Primary ID: 08594072958502

PAN7.18 Bandáž kolenní XL (UDI 08594072958502)

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 PAN7.18 Bandáž kolenní XL - Primary ID 08594072958502

Device Regulatory Overview

The PAN7.18 Bandáž kolenní XL (Model/Catalog Number: PAN7.18 XL) is a medical device manufactured by PANOP CZ s.r.o.. This product is indexed under FDA Product Code / Category Classification M030299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PAN7.18 XL
Product Code / EMDN
M030299
Device Name
Bandáž kolenní
Database Sync Date
2026-08-09 16:50:47

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 PAN7.18 Bandáž kolenní XL?

The registered manufacturer of record for PAN7.18 Bandáž kolenní XL is PANOP CZ s.r.o..

What is the Primary UDI-DI identifier for PAN7.18 Bandáž kolenní XL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594072958502.

What classification code is assigned to this device?

This device is registered under product classification code M030299.

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