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Mark3

FDA UDI

Class II (US FDA UDI)

by Cargus International, Inc

Identity

Trade Name
MARK3 FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
Permanent Resin Cement Dual Cure 8gm. Automix Syringe + Mixing Tips - MARK3® FDA UDI
Model / Reference
5385 FDA UDI
Description
Permanent Resin Cement Dual Cure 8gm. Automix Syringe + Mixing Tips - MARK3® FDA UDI

Identifiers

Catalog Number
5385 FDA UDI
Primary DI / UDI-DI
D79653851 FDA UDI
FDA Product Code
KLE FDA UDI
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental composite resinDental material mixing nozzle

Mark3 by Cargus International, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental material mixing nozzle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 12a8194b-1a84-47e4-92dd-4ebe199ebcd8 35 fields · synced Jun 1, 2026