GUDIDData
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eudamed_udi Primary ID: 08058481761578

CARROZZINA PIEGHEVOLE PMN EXTREME PLUS 43 (UDI 08058481761578)

Manufactured by PRAXIS MEDICAL NETWORK SRL

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CARROZZINA PIEGHEVOLE PMN EXTREME PLUS 43 - Primary ID 08058481761578

Device Regulatory Overview

The CARROZZINA PIEGHEVOLE PMN EXTREME PLUS 43 (Model/Catalog Number: PX17010) is a medical device manufactured by PRAXIS MEDICAL NETWORK SRL. This product is indexed under FDA Product Code / Category Classification Y122106 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PX17010
Product Code / EMDN
Y122106
Device Name
CARROZZINE STANDARD PMN
Database Sync Date
2026-08-09 16:49:01

Full Regulatory Attributes

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{
    "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 CARROZZINA PIEGHEVOLE PMN EXTREME PLUS 43?

The registered manufacturer of record for CARROZZINA PIEGHEVOLE PMN EXTREME PLUS 43 is PRAXIS MEDICAL NETWORK SRL.

What is the Primary UDI-DI identifier for CARROZZINA PIEGHEVOLE PMN EXTREME PLUS 43?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058481761578.

What classification code is assigned to this device?

This device is registered under product classification code Y122106.

Similar Classification Devices (Y122106)

Other Devices by PRAXIS MEDICAL NETWORK SRL

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