GUDIDData
eudamed_udi Primary ID: 08016867020329

Presteril Sicura Assorbenti ripiegati in cotone NORMAL per perdite urinarie (UDI 08016867020329)

Manufactured by CORMAN S.p.A.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Presteril Sicura Assorbenti ripiegati in cotone NORMAL per perdite urinarie - Primary ID 08016867020329

Device Regulatory Overview

The Presteril Sicura Assorbenti ripiegati in cotone NORMAL per perdite urinarie (Model/Catalog Number: PLAINC02) is a medical device manufactured by CORMAN S.p.A.. This product is indexed under FDA Product Code / Category Classification T04010102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PLAINC02
Product Code / EMDN
T04010102
Device Name
Assorbenti per perdite urinarie
Database Sync Date
2026-08-09 16:49:52

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 Presteril Sicura Assorbenti ripiegati in cotone NORMAL per perdite urinarie?

The registered manufacturer of record for Presteril Sicura Assorbenti ripiegati in cotone NORMAL per perdite urinarie is CORMAN S.p.A..

What is the Primary UDI-DI identifier for Presteril Sicura Assorbenti ripiegati in cotone NORMAL per perdite urinarie?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08016867020329.

What classification code is assigned to this device?

This device is registered under product classification code T04010102.

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