GUDIDData
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eudamed_udi Primary ID: 08058481761189

SEDILE GIREVOLE PER VASCA DA BAGNO A LARGHEZZA REGOLABILE IN ALLUMINIO VERNICIATO BIANCO (UDI 08058481761189)

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 GIREVOLE PER VASCA DA BAGNO A LARGHEZZA REGOLABILE IN ALLUMINIO VERNICIATO BIANCO - Primary ID 08058481761189

Device Regulatory Overview

The SEDILE GIREVOLE PER VASCA DA BAGNO A LARGHEZZA REGOLABILE IN ALLUMINIO VERNICIATO BIANCO (Model/Catalog Number: PX16239) 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
PX16239
Product Code / EMDN
Y093303
Device Name
SEDILI GIREVOLI PER VASCA
Database Sync Date
2026-08-09 16:29:55

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 SEDILE GIREVOLE PER VASCA DA BAGNO A LARGHEZZA REGOLABILE IN ALLUMINIO VERNICIATO BIANCO?

The registered manufacturer of record for SEDILE GIREVOLE PER VASCA DA BAGNO A LARGHEZZA REGOLABILE IN ALLUMINIO VERNICIATO BIANCO is PRAXIS MEDICAL NETWORK SRL.

What is the Primary UDI-DI identifier for SEDILE GIREVOLE PER VASCA DA BAGNO A LARGHEZZA REGOLABILE IN ALLUMINIO VERNICIATO BIANCO?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058481761189.

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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