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LuxaFlow® Ultra BL

FDA UDI

Class II (US FDA UDI)

by DMG Chemisch-Pharmazeutische Fabrik GmbH

Identity

Trade Name
LuxaFlow® Ultra BL FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
Flowable light cure provisional add-on material Refill Content: 2 Syringes @ 1.5 g, 10 Luer-Lock-Tips. Color: BL FDA UDI
Model / Reference
224008 FDA UDI
Description
Flowable light cure provisional add-on material Refill Content: 2 Syringes @ 1.5 g, 10 Luer-Lock-Tips. Color: BL FDA UDI

Identifiers

Catalog Number
224008 FDA UDI
Primary DI / UDI-DI
EDMG2240080 FDA UDI
510(k) Number
K011211 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3690 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental composite resin

LuxaFlow® Ultra BL by DMG Chemisch-Pharmazeutische Fabrik GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ca1dd72b-5e44-446f-921d-2f3f4adb9d92 36 fields · synced May 30, 2026