GUDIDData
eudamed_udi Primary ID: 08058481762827

CILINDRO PER CUSCINETTO A SFERE RUOTA 12" PER CARROZZINE EXTREME TR (I) (UDI 08058481762827)

Manufactured by PRAXIS MEDICAL NETWORK SRL

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CILINDRO PER CUSCINETTO A SFERE RUOTA 12" PER CARROZZINE EXTREME TR (I) - Primary ID 08058481762827

Device Regulatory Overview

The CILINDRO PER CUSCINETTO A SFERE RUOTA 12" PER CARROZZINE EXTREME TR (I) (Model/Catalog Number: PX17R034-1I) is a medical device manufactured by PRAXIS MEDICAL NETWORK SRL. This product is indexed under FDA Product Code / Category Classification Y122499 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PX17R034-1I
Product Code / EMDN
Y122499
Device Name
RICAMBI CARROZZINE STANDARD
Database Sync Date
2026-08-09 16:28:44

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 CILINDRO PER CUSCINETTO A SFERE RUOTA 12" PER CARROZZINE EXTREME TR (I)?

The registered manufacturer of record for CILINDRO PER CUSCINETTO A SFERE RUOTA 12" PER CARROZZINE EXTREME TR (I) is PRAXIS MEDICAL NETWORK SRL.

What is the Primary UDI-DI identifier for CILINDRO PER CUSCINETTO A SFERE RUOTA 12" PER CARROZZINE EXTREME TR (I)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058481762827.

What classification code is assigned to this device?

This device is registered under product classification code Y122499.

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