GUDIDData
eudamed_udi Primary ID: 08001480506916

LINES SPECIALIST ASSORBENTE ANATOMICO MAXI NIGHT (UDI 08001480506916)

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 ASSORBENTE ANATOMICO MAXI NIGHT - Primary ID 08001480506916

Device Regulatory Overview

The LINES SPECIALIST ASSORBENTE ANATOMICO MAXI NIGHT (Model/Catalog Number: 8001480506916 ) is a medical device manufactured by Fater S.p.A.. This product is indexed under FDA Product Code / Category Classification T0499 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
8001480506916 
Product Code / EMDN
T0499
Device Name
ASSORBENTE
Database Sync Date
2026-08-09 17:07:49

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 LINES SPECIALIST ASSORBENTE ANATOMICO MAXI NIGHT?

The registered manufacturer of record for LINES SPECIALIST ASSORBENTE ANATOMICO MAXI NIGHT is Fater S.p.A..

What is the Primary UDI-DI identifier for LINES SPECIALIST ASSORBENTE ANATOMICO MAXI NIGHT?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08001480506916.

What classification code is assigned to this device?

This device is registered under product classification code T0499.

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