eudamed_udi Primary ID: 08594072958977

PAN1.03 Límec krční kuličkový XL (UDI 08594072958977)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The PAN1.03 Límec krční kuličkový XL (Model/Catalog Number: PAN1.03 XL) is a medical device manufactured by PANOP CZ s.r.o.. This product is indexed under FDA Product Code / Category Classification Y060312 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: PAN1.03 XL
Product Code / EMDN: Y060312
Device Name: Límec krční kuličkový
Database Sync Date: 2026-08-09 16:45:59

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 PAN1.03 Límec krční kuličkový XL?

The registered manufacturer of record for PAN1.03 Límec krční kuličkový XL is PANOP CZ s.r.o..

What is the Primary UDI-DI identifier for PAN1.03 Límec krční kuličkový XL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594072958977.

What classification code is assigned to this device?

This device is registered under product classification code Y060312.

Similar Classification Devices (Y060312)

Other Devices by PANOP CZ s.r.o.

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