GUDIDData
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eudamed_udi Primary ID: 08058481760793

SEDILE PER DOCCIA IN ALLUMINIO SENZA SCHIENALE - REGOLABILE IN ALTEZZA (UDI 08058481760793)

Manufactured by PRAXIS MEDICAL NETWORK SRL

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SEDILE PER DOCCIA IN ALLUMINIO SENZA SCHIENALE - REGOLABILE IN ALTEZZA - Primary ID 08058481760793

Device Regulatory Overview

The SEDILE PER DOCCIA IN ALLUMINIO SENZA SCHIENALE - REGOLABILE IN ALTEZZA (Model/Catalog Number: PX16200) is a medical device manufactured by PRAXIS MEDICAL NETWORK SRL. This product is indexed under FDA Product Code / Category Classification Y093303 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PX16200
Product Code / EMDN
Y093303
Device Name
SEDILI PER DOCCIA
Database Sync Date
2026-08-09 16:59:13

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 SEDILE PER DOCCIA IN ALLUMINIO SENZA SCHIENALE - REGOLABILE IN ALTEZZA?

The registered manufacturer of record for SEDILE PER DOCCIA IN ALLUMINIO SENZA SCHIENALE - REGOLABILE IN ALTEZZA is PRAXIS MEDICAL NETWORK SRL.

What is the Primary UDI-DI identifier for SEDILE PER DOCCIA IN ALLUMINIO SENZA SCHIENALE - REGOLABILE IN ALTEZZA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058481760793.

What classification code is assigned to this device?

This device is registered under product classification code Y093303.

Similar Classification Devices (Y093303)

Other Devices by PRAXIS MEDICAL NETWORK SRL

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