GUDIDData
eudamed_udi Primary ID: 04251952220909

BevistoSept plus Wipes 12 x Dose mit je 120 Tüchern (UDI 04251952220909)

Manufactured by BEVISTON GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BevistoSept plus Wipes 12 x Dose mit je 120 Tüchern - Primary ID 04251952220909

Device Regulatory Overview

The BevistoSept plus Wipes 12 x Dose mit je 120 Tüchern (Model/Catalog Number: 2090) is a medical device manufactured by BEVISTON GmbH. This product is indexed under FDA Product Code / Category Classification D0701 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
2090
Product Code / EMDN
D0701
Device Name
BevistoSept plus
Database Sync Date
2026-08-09 16:30:11

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 BevistoSept plus Wipes 12 x Dose mit je 120 Tüchern?

The registered manufacturer of record for BevistoSept plus Wipes 12 x Dose mit je 120 Tüchern is BEVISTON GmbH.

What is the Primary UDI-DI identifier for BevistoSept plus Wipes 12 x Dose mit je 120 Tüchern?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251952220909.

What classification code is assigned to this device?

This device is registered under product classification code D0701.

Programmatic Export

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

JSON API Endpoint