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Mark3

FDA UDI

Class II (US FDA UDI)

by Cargus International, Inc

Identity

Trade Name
MARK3 FDA UDI
Generic Name
Sterilization container liner FDA UDI
Device Name
Self Seal 2-1/4" x 5" (2-1/4" x 4") Sterilization Pouches 60/cs. - MARK3 FDA UDI
Model / Reference
6110CS FDA UDI
Description
Self Seal 2-1/4" x 5" (2-1/4" x 4") Sterilization Pouches 60/cs. - MARK3 FDA UDI

Identifiers

Primary DI / UDI-DI
D7966110CS1 FDA UDI
FDA Product Code
FRG FDA UDI
JOJ FDA UDI
GMDN Term
Sterilization container liner FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 FDA UDI
880.2800 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Sterilization container liner

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

Similar devices

Also classified as Sterilization container liner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cargus International, Inc

Sources (1)

  • FDA UDI 8c20b6fa-8009-4cdc-8a11-4656465d4ffc 34 fields · synced May 30, 2026