gudid
Primary ID: 171620
LuxaPrint Ortho NX 385 nm (UDI 171620)
Manufactured by DMG Digital Enterprises SE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LuxaPrint Ortho NX 385 nm - Primary ID 171620
Device Regulatory Overview
The LuxaPrint Ortho NX 385 nm (Model/Catalog Number: 171620) is a medical device manufactured by DMG Digital Enterprises SE. This product is indexed under FDA Product Code / Category Classification DYT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 171620
- Product Code / EMDN
- DYT
- Device Name
- Light-curing resin based on (meth)acrylate for the production of dental devices. For DLP/ SLA printers that work at wavelengths of 385 nm and 405 nm. Content: 1 Bottle @ 200 g
- Database Sync Date
- 2026-08-09 09:01:10
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 LuxaPrint Ortho NX 385 nm?
The registered manufacturer of record for LuxaPrint Ortho NX 385 nm is DMG Digital Enterprises SE.
What is the Primary UDI-DI identifier for LuxaPrint Ortho NX 385 nm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 171620.
What classification code is assigned to this device?
This device is registered under product classification code DYT.
Similar Classification Devices (DYT)
Other Devices by DMG Digital Enterprises SE
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint