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Mark3

FDA UDI

Class I (US FDA UDI)

by Cargus International, Inc

Identity

Trade Name
MARK3 FDA UDI
Generic Name
Dentifrice FDA UDI
Device Name
Prophy Paste Coarse Cherry 200/bx. - MARK3® FDA UDI
Model / Reference
1532 FDA UDI
Description
Prophy Paste Coarse Cherry 200/bx. - MARK3® FDA UDI

Identifiers

Primary DI / UDI-DI
D796415321 FDA UDI
FDA Product Code
EJR FDA UDI
GMDN Term
Dentifrice FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6030 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dentifrice

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

Similar devices

Also classified as Dentifrice.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dc40074e-4a60-4fcb-bb0d-1b5396d240f7 34 fields · synced May 30, 2026