GUDIDData
eudamed_udi Primary ID: 08001480504646

LINES SPECIALIST DERMA PROTECTION PANNOLONE A MUTANDINA MAXI MIS. GRANDE (UDI 08001480504646)

Manufactured by Fater S.p.A.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LINES SPECIALIST DERMA PROTECTION PANNOLONE A MUTANDINA MAXI MIS. GRANDE - Primary ID 08001480504646

Device Regulatory Overview

The LINES SPECIALIST DERMA PROTECTION PANNOLONE A MUTANDINA MAXI MIS. GRANDE (Model/Catalog Number: 8001480504646) is a medical device manufactured by Fater S.p.A.. This product is indexed under FDA Product Code / Category Classification T04010103 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
8001480504646
Product Code / EMDN
T04010103
Device Name
PANNOLONE A MUTANDINA (BRIEF)
Database Sync Date
2026-08-09 16:29:18

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of LINES SPECIALIST DERMA PROTECTION PANNOLONE A MUTANDINA MAXI MIS. GRANDE?

The registered manufacturer of record for LINES SPECIALIST DERMA PROTECTION PANNOLONE A MUTANDINA MAXI MIS. GRANDE is Fater S.p.A..

What is the Primary UDI-DI identifier for LINES SPECIALIST DERMA PROTECTION PANNOLONE A MUTANDINA MAXI MIS. GRANDE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08001480504646.

What classification code is assigned to this device?

This device is registered under product classification code T04010103.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint