GUDIDData
gudid Primary ID: 1.013.4800

elements e-motion (UDI 1.013.4800)

Manufactured by KaVo Dental GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for elements e-motion - Primary ID 1.013.4800

Device Regulatory Overview

The elements e-motion (Model/Catalog Number: 1.013.4800) is a medical device manufactured by KaVo Dental GmbH. This product is indexed under FDA Product Code / Category Classification EBW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1.013.4800
Product Code / EMDN
EBW
Device Name
The dental treatment unit running as a desktop unit is intended for use in the field of dentistry. It is designed for the operation of an electrically operated small voltage motor. Area of application is in the field of endodontics and tooth preparation.
Database Sync Date
2026-08-09 09:08:27

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 elements e-motion?

The registered manufacturer of record for elements e-motion is KaVo Dental GmbH.

What is the Primary UDI-DI identifier for elements e-motion?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.013.4800.

What classification code is assigned to this device?

This device is registered under product classification code EBW.

Programmatic Export

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

JSON API Endpoint