LuxaPrint Ortho Plus 385 (UDI 171259)
Manufactured by DMG Chemisch-Pharmazeutische Fabrik GmbH
Device Regulatory Overview
The LuxaPrint Ortho Plus 385 (Model/Catalog Number: 171259) is a medical device manufactured by DMG Chemisch-Pharmazeutische Fabrik GmbH. This product is indexed under FDA Product Code / Category Classification MQC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 171259
- Product Code / EMDN
- MQC
- Device Name
- (Meth) acrylate-based light-curing resin exclusively for use in the dental laboratory. For DLP/ STL printers at a wavelength of 385 nm. High spirits in 3D. Content: 1 Bottle @ 200 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 Ortho Plus 385?
The registered manufacturer of record for LuxaPrint Ortho Plus 385 is DMG Chemisch-Pharmazeutische Fabrik GmbH.
What is the Primary UDI-DI identifier for LuxaPrint Ortho Plus 385?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 171259.
What classification code is assigned to this device?
This device is registered under product classification code MQC.
Similar Classification Devices (MQC)
Other Devices by DMG Chemisch-Pharmazeutische Fabrik GmbH
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