GUDIDData
eudamed_udi Primary ID: 08032472006831

Neobianacid (UDI 08032472006831)

Manufactured by ABOCA S.P.A. SOCIETÀ AGRICOLA

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Neobianacid - Primary ID 08032472006831

Device Regulatory Overview

The Neobianacid (Model/Catalog Number: 08032472006831) is a medical device manufactured by ABOCA S.P.A. SOCIETÀ AGRICOLA. This product is indexed under FDA Product Code / Category Classification G0401 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
08032472006831
Product Code / EMDN
G0401
Device Name
Neobianacid
Database Sync Date
2026-08-09 16:28:55

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 Neobianacid?

The registered manufacturer of record for Neobianacid is ABOCA S.P.A. SOCIETÀ AGRICOLA.

What is the Primary UDI-DI identifier for Neobianacid?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08032472006831.

What classification code is assigned to this device?

This device is registered under product classification code G0401.

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