GUDIDData
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eudamed_udi Primary ID: 08058481765118

FRENO ALLUMINIO SINISTRO PER CARROZZINA PMN ACTIVA / ACTIVA TR (UDI 08058481765118)

Manufactured by PRAXIS MEDICAL NETWORK SRL

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FRENO ALLUMINIO SINISTRO PER CARROZZINA PMN ACTIVA / ACTIVA TR - Primary ID 08058481765118

Device Regulatory Overview

The FRENO ALLUMINIO SINISTRO PER CARROZZINA PMN ACTIVA / ACTIVA TR (Model/Catalog Number: PX17R081) 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
PX17R081
Product Code / EMDN
Y122499
Device Name
RICAMBI CARROZZINE LEGGERE
Database Sync Date
2026-08-09 16:58:31

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 FRENO ALLUMINIO SINISTRO PER CARROZZINA PMN ACTIVA / ACTIVA TR?

The registered manufacturer of record for FRENO ALLUMINIO SINISTRO PER CARROZZINA PMN ACTIVA / ACTIVA TR is PRAXIS MEDICAL NETWORK SRL.

What is the Primary UDI-DI identifier for FRENO ALLUMINIO SINISTRO PER CARROZZINA PMN ACTIVA / ACTIVA TR?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058481765118.

What classification code is assigned to this device?

This device is registered under product classification code Y122499.

Similar Classification Devices (Y122499)

Other Devices by PRAXIS MEDICAL NETWORK SRL

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