GUDIDData
eudamed_udi Primary ID: 08057509262172

Federa medicale in polipropilene (UDI 08057509262172)

Manufactured by IDS S.r.l.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Federa medicale in polipropilene - Primary ID 08057509262172

Device Regulatory Overview

The Federa medicale in polipropilene (Model/Catalog Number: ID-P-W) is a medical device manufactured by IDS S.r.l.. This product is indexed under FDA Product Code / Category Classification T030502 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ID-P-W
Product Code / EMDN
T030502
Device Name
Federa medicale in polipropilene
Database Sync Date
2026-08-09 17:19:38

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 Federa medicale in polipropilene?

The registered manufacturer of record for Federa medicale in polipropilene is IDS S.r.l..

What is the Primary UDI-DI identifier for Federa medicale in polipropilene?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08057509262172.

What classification code is assigned to this device?

This device is registered under product classification code T030502.

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