GUDIDData
eudamed_udi Primary ID: 04099637006413

Prophy-Brush Kelch normal flach 50er (UDI 04099637006413)

Manufactured by Hager & Werken GmbH & Co. KG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Prophy-Brush Kelch normal flach 50er - Primary ID 04099637006413

Device Regulatory Overview

The Prophy-Brush Kelch normal flach 50er (Model/Catalog Number: 605871) is a medical device manufactured by Hager & Werken GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification Q019006 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
605871
Product Code / EMDN
Q019006
Device Name
Polierbürsten, dental
Database Sync Date
2026-08-09 16:29:26

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 Prophy-Brush Kelch normal flach 50er?

The registered manufacturer of record for Prophy-Brush Kelch normal flach 50er is Hager & Werken GmbH & Co. KG.

What is the Primary UDI-DI identifier for Prophy-Brush Kelch normal flach 50er?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04099637006413.

What classification code is assigned to this device?

This device is registered under product classification code Q019006.

Programmatic Export

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

JSON API Endpoint