GUDIDData
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eudamed_udi Primary ID: 08058481763398

FASCIA FERMAGAMBE PEDANA PER CARROZZINE EXTREME/EXTREME TR (UDI 08058481763398)

Manufactured by PRAXIS MEDICAL NETWORK SRL

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FASCIA FERMAGAMBE PEDANA PER CARROZZINE EXTREME/EXTREME TR - Primary ID 08058481763398

Device Regulatory Overview

The FASCIA FERMAGAMBE PEDANA PER CARROZZINE EXTREME/EXTREME TR (Model/Catalog Number: PX17R068) 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
PX17R068
Product Code / EMDN
Y122403
Device Name
RICAMBI CARROZZINE STANDARD
Database Sync Date
2026-08-09 17:03:20

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 FASCIA FERMAGAMBE PEDANA PER CARROZZINE EXTREME/EXTREME TR?

The registered manufacturer of record for FASCIA FERMAGAMBE PEDANA PER CARROZZINE EXTREME/EXTREME TR is PRAXIS MEDICAL NETWORK SRL.

What is the Primary UDI-DI identifier for FASCIA FERMAGAMBE PEDANA PER CARROZZINE EXTREME/EXTREME TR?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058481763398.

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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