GUDIDData
eudamed_udi Primary ID: 03831131424307

MEDICO ANTIDECUBITUS (UDI 03831131424307)

Manufactured by PURO TEHNIKA PODJETJE ZA PREDELAVO IN TRŽENJE POLIURETANSKE PENE D.O.O.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MEDICO ANTIDECUBITUS - Primary ID 03831131424307

Device Regulatory Overview

The MEDICO ANTIDECUBITUS (Model/Catalog Number: 053) is a medical device manufactured by PURO TEHNIKA PODJETJE ZA PREDELAVO IN TRŽENJE POLIURETANSKE PENE D.O.O.. This product is indexed under FDA Product Code / Category Classification V08030102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
053
Product Code / EMDN
V08030102
Device Name
MEDICINSKI POSTELJNI VLOŽEK MEDICO ANTIDECUBITUS
Database Sync Date
2026-08-09 16:29:04

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 MEDICO ANTIDECUBITUS?

The registered manufacturer of record for MEDICO ANTIDECUBITUS is PURO TEHNIKA PODJETJE ZA PREDELAVO IN TRŽENJE POLIURETANSKE PENE D.O.O..

What is the Primary UDI-DI identifier for MEDICO ANTIDECUBITUS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03831131424307.

What classification code is assigned to this device?

This device is registered under product classification code V08030102.

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