← Back to catalogue

Mark3

FDA UDI

Class I (US FDA UDI)

by Cargus International, Inc

Identity

Trade Name
MARK3 FDA UDI
Generic Name
Non-woven gauze pad, non-sterile FDA UDI
Device Name
Sponges Non Woven Non Sterile 2" x 2" 4Ply 5000/cs. - MARK3 FDA UDI
Model / Reference
2224 FDA UDI
Description
Sponges Non Woven Non Sterile 2" x 2" 4Ply 5000/cs. - MARK3 FDA UDI

Identifiers

Primary DI / UDI-DI
D79622241 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Non-woven gauze pad, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Non-woven gauze pad, non-sterile

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

Similar devices

Also classified as Non-woven gauze pad, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI e5804645-5583-4cfa-920e-dd60bcf7532f 34 fields · synced Jun 8, 2026