GUDIDData
eudamed_udi Primary ID: 08058481764203

SET DUE GAMBE CON RUOTE 3" PVC PIROETTANTI PER DEAMBULATORE ALLUMINIO (UDI 08058481764203)

Manufactured by PRAXIS MEDICAL NETWORK SRL

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SET DUE GAMBE CON RUOTE 3" PVC PIROETTANTI PER DEAMBULATORE ALLUMINIO - Primary ID 08058481764203

Device Regulatory Overview

The SET DUE GAMBE CON RUOTE 3" PVC PIROETTANTI PER DEAMBULATORE ALLUMINIO (Model/Catalog Number: PX1801B) is a medical device manufactured by PRAXIS MEDICAL NETWORK SRL. This product is indexed under FDA Product Code / Category Classification Y120680 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PX1801B
Product Code / EMDN
Y120680
Device Name
ACCESSORI PER DEAMBULATORI PMN
Database Sync Date
2026-08-09 16:28:59

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 SET DUE GAMBE CON RUOTE 3" PVC PIROETTANTI PER DEAMBULATORE ALLUMINIO?

The registered manufacturer of record for SET DUE GAMBE CON RUOTE 3" PVC PIROETTANTI PER DEAMBULATORE ALLUMINIO is PRAXIS MEDICAL NETWORK SRL.

What is the Primary UDI-DI identifier for SET DUE GAMBE CON RUOTE 3" PVC PIROETTANTI PER DEAMBULATORE ALLUMINIO?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058481764203.

What classification code is assigned to this device?

This device is registered under product classification code Y120680.

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