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Mark3

FDA UDI

Class I (US FDA UDI)

by Cargus International, Inc

Identity

Trade Name
MARK3 FDA UDI
Generic Name
Dappen dish, reusable FDA UDI
Device Name
Dappen Dish Glass Blue 12/bx. - MARK3®* FDA UDI
Model / Reference
2615 FDA UDI
Description
Dappen Dish Glass Blue 12/bx. - MARK3®* FDA UDI

Identifiers

Catalog Number
2615 FDA UDI
Primary DI / UDI-DI
D79626151 FDA UDI
FDA Product Code
JDZ FDA UDI
GMDN Term
Dappen dish, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4210 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dappen dish, reusable

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

Similar devices

Also classified as Dappen dish, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b33307e8-60e1-40d0-9fbf-0161432b22a9 35 fields · synced May 30, 2026