eudamed_udi Primary ID: 05903940706238

PAS BRZUSZNY "24CM" VENTRIMAX (UDI 05903940706238)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The PAS BRZUSZNY "24CM" VENTRIMAX (Model/Catalog Number: O-1400/XL) is a medical device manufactured by REHA FUND Sp. z o.o.. This product is indexed under FDA Product Code / Category Classification Y060499 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: O-1400/XL
Product Code / EMDN: Y060499
Device Name: Pas brzuszny "24cm" Ventrimax
Database Sync Date: 2026-08-09 16:29:50

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 PAS BRZUSZNY "24CM" VENTRIMAX?

The registered manufacturer of record for PAS BRZUSZNY "24CM" VENTRIMAX is REHA FUND Sp. z o.o..

What is the Primary UDI-DI identifier for PAS BRZUSZNY "24CM" VENTRIMAX?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05903940706238.

What classification code is assigned to this device?

This device is registered under product classification code Y060499.

Similar Classification Devices (Y060499)

Other Devices by REHA FUND Sp. z o.o.

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