LuxaPrint Ortho Plus 405

FDA UDI

Class U (US FDA UDI)

by DMG Digital Enterprises SE

Identity

Trade Name: LuxaPrint Ortho Plus 405 FDA UDI
Generic Name: Dental appliance fabrication material, resin FDA UDI
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 @ 200 g FDA UDI
Model / Reference: 171260 FDA UDI
Description: (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 @ 200 g FDA UDI

Identifiers

Catalog Number: 171260 FDA UDI
Primary DI / UDI-DI: D9821712600 FDA UDI
FDA Product Code: MQC FDA UDI
EBI FDA UDI
GMDN Term: Dental appliance fabrication material, resin FDA UDI

Classification

Device Class: U FDA UDI
Regulation Number: 872.3760 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Dental appliance fabrication material, resin

LuxaPrint Ortho Plus 405 by DMG Digital Enterprises SE — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class U	Pending data

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Manufacturer

Manufacturer: DMG Digital Enterprises SE

Sources (1)

FDA UDI ed4e3869-8bc0-41b7-aab3-f8c930ae3bda 36 fields · synced May 30, 2026