eudamed_udi Primary ID: 08594072956461

PAN3.07 Pás břišní nízký XXL (UDI 08594072956461)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The PAN3.07 Pás břišní nízký XXL (Model/Catalog Number: PAN3.07/I/XXL) 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: PAN3.07/I/XXL
Product Code / EMDN: M030299
Device Name: Pás břišní
Database Sync Date: 2026-08-09 18:42:45

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of PAN3.07 Pás břišní nízký XXL?

The registered manufacturer of record for PAN3.07 Pás břišní nízký XXL is PANOP CZ s.r.o..

What is the Primary UDI-DI identifier for PAN3.07 Pás břišní nízký XXL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594072956461.

What classification code is assigned to this device?

This device is registered under product classification code M030299.

Similar Classification Devices (M030299)

Other Devices by PANOP CZ s.r.o.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint