GUDIDData
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eudamed_udi Primary ID: 08058481762650

PEDANE ALLUMINIO ESTRAIBILI (DX+SX) (TELAIO+PEDANA PLASTICA) CARROZZINE PMN ACTIVA COLORE BURGUNDY (UDI 08058481762650)

Manufactured by PRAXIS MEDICAL NETWORK SRL

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PEDANE ALLUMINIO ESTRAIBILI (DX+SX) (TELAIO+PEDANA PLASTICA) CARROZZINE PMN ACTIVA COLORE BURGUNDY - Primary ID 08058481762650

Device Regulatory Overview

The PEDANE ALLUMINIO ESTRAIBILI (DX+SX) (TELAIO+PEDANA PLASTICA) CARROZZINE PMN ACTIVA COLORE BURGUNDY (Model/Catalog Number: PX17R024I) is a medical device manufactured by PRAXIS MEDICAL NETWORK SRL. This product is indexed under FDA Product Code / Category Classification Y122403 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PX17R024I
Product Code / EMDN
Y122403
Device Name
RICAMBI CARROZZINE LEGGERE
Database Sync Date
2026-08-09 16:30:02

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 PEDANE ALLUMINIO ESTRAIBILI (DX+SX) (TELAIO+PEDANA PLASTICA) CARROZZINE PMN ACTIVA COLORE BURGUNDY?

The registered manufacturer of record for PEDANE ALLUMINIO ESTRAIBILI (DX+SX) (TELAIO+PEDANA PLASTICA) CARROZZINE PMN ACTIVA COLORE BURGUNDY is PRAXIS MEDICAL NETWORK SRL.

What is the Primary UDI-DI identifier for PEDANE ALLUMINIO ESTRAIBILI (DX+SX) (TELAIO+PEDANA PLASTICA) CARROZZINE PMN ACTIVA COLORE BURGUNDY?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058481762650.

What classification code is assigned to this device?

This device is registered under product classification code Y122403.

Similar Classification Devices (Y122403)

Other Devices by PRAXIS MEDICAL NETWORK SRL

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