← Back to catalogue

Cardinal Health

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
CARDINAL HEALTH FDA UDI
Generic Name
Non-woven gauze pad, non-sterile FDA UDI
Device Name
Gauze Sponges 2 x 2in. (5.1 x 5.1cm) 8-Ply • Woven 100 percent Cotton • Non Sterile. Single Use Only. Not Made with Natural Rubber Latex. Store in a Cool, Dry Place. FDA UDI
Model / Reference
C-NSG228E FDA UDI
Description
Gauze Sponges 2 x 2in. (5.1 x 5.1cm) 8-Ply • Woven 100 percent Cotton • Non Sterile. Single Use Only. Not Made with Natural Rubber Latex. Store in a Cool, Dry Place. FDA UDI

Identifiers

Catalog Number
C-NSG228E FDA UDI
Primary DI / UDI-DI
20885380066600 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

Yes

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: Non-woven gauze pad, non-sterile

Cardinal Health by Cardinal Health 200, LLC — 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 f448d647-454b-43b7-9d90-ad24c945cf9a 34 fields · synced Jun 8, 2026