LuxaPost

FDA UDI

Class I (US FDA UDI)

by DMG Chemisch-Pharmazeutische Fabrik GmbH

Identity

Trade Name: LuxaPost FDA UDI
Generic Name: Root canal post kit FDA UDI
Device Name: Core-build-up and post cementation. Content: 5 posts Ø 1.25 mm, 5 posts Ø 1.375 mm, 5 posts Ø 1.5 mm, 1 drill Ø 1.25 mm, 1 drill Ø 1.375 mm, 1 drill Ø 1.5 mm, 30 silicone stops. FDA UDI
Model / Reference: 110780 FDA UDI
Description: Core-build-up and post cementation. Content: 5 posts Ø 1.25 mm, 5 posts Ø 1.375 mm, 5 posts Ø 1.5 mm, 1 drill Ø 1.25 mm, 1 drill Ø 1.375 mm, 1 drill Ø 1.5 mm, 30 silicone stops. FDA UDI

Identifiers

Catalog Number: 110780 FDA UDI
Primary DI / UDI-DI: EDMG1107801 FDA UDI
FDA Product Code: ELR FDA UDI
GMDN Term: Root canal post kit FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.3810 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Liquid Chemical FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 1.25 Millimeter FDA UDI
Outer Diameter — 1.375 Millimeter FDA UDI
Outer Diameter — 1.5 Millimeter FDA UDI

Category: Root canal post kit

LuxaPost by DMG Chemisch-Pharmazeutische Fabrik GmbH — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: DMG Chemisch-Pharmazeutische Fabrik GmbH

Sources (1)

FDA UDI 1f350ccc-d212-4547-8a1c-e75964d56f36 37 fields · synced May 30, 2026