gudid
Primary ID: 171205
LuxaPrint Tray (UDI 171205)
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 LuxaPrint Tray - Primary ID 171205
Device Regulatory Overview
The LuxaPrint Tray (Model/Catalog Number: 171205) is a medical device manufactured by DMG Chemisch-Pharmazeutische Fabrik GmbH. This product is indexed under FDA Product Code / Category Classification EBH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 171205
- Product Code / EMDN
- EBH
- Device Name
- (Meth) acrylate-based light-curing resin exclusively for use in the dental laboratory. For DLP/ STL printers at a wavelength of 405 nm or 385 nm. High spirits in 3D. Content: 1 Bottle @ 1000 g
- Database Sync Date
- 2026-08-09 09:01:10
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 LuxaPrint Tray?
The registered manufacturer of record for LuxaPrint Tray is DMG Chemisch-Pharmazeutische Fabrik GmbH.
What is the Primary UDI-DI identifier for LuxaPrint Tray?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 171205.
What classification code is assigned to this device?
This device is registered under product classification code EBH.
Similar Classification Devices (EBH)
Other Devices by DMG Chemisch-Pharmazeutische Fabrik GmbH
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