gudid
Primary ID: 224002
LuxaFlow Ultra (UDI 224002)
Manufactured by DMG Chemisch-Pharmazeutische Fabrik GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LuxaFlow Ultra - Primary ID 224002
Device Regulatory Overview
The LuxaFlow Ultra (Model/Catalog Number: 224002) is a medical device manufactured by DMG Chemisch-Pharmazeutische Fabrik GmbH. This product is indexed under FDA Product Code / Category Classification EBF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 224002
- Product Code / EMDN
- EBF
- Device Name
- Flowable light cure provisional add-on material. Esthetic add-ons and repairs. Content: 2 syringes @ 1.5 g composite, Accessories. Color: A2
- Database Sync Date
- 2026-08-09 09:23:50
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of LuxaFlow Ultra?
The registered manufacturer of record for LuxaFlow Ultra is DMG Chemisch-Pharmazeutische Fabrik GmbH.
What is the Primary UDI-DI identifier for LuxaFlow Ultra?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 224002.
What classification code is assigned to this device?
This device is registered under product classification code EBF.
Similar Classification Devices (EBF)
Other Devices by DMG Chemisch-Pharmazeutische Fabrik GmbH
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