GUDIDData
gudid Primary ID: 1.003.5840

ELECTROtorque TLC 4893 (Set) (UDI 1.003.5840)

Manufactured by KaVo Dental GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ELECTROtorque TLC 4893 (Set) - Primary ID 1.003.5840

Device Regulatory Overview

The ELECTROtorque TLC 4893 (Set) (Model/Catalog Number: 1.003.5840) 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
1.003.5840
Product Code / EMDN
EBW
Device Name
This is a medical device.
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 ELECTROtorque TLC 4893 (Set)?

The registered manufacturer of record for ELECTROtorque TLC 4893 (Set) is KaVo Dental GmbH.

What is the Primary UDI-DI identifier for ELECTROtorque TLC 4893 (Set)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.003.5840.

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