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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
Premium Gauze Sponges 2 x 2in. (5.1 x 5.1cm) 8 Ply. Woven 100 percent Cotton. CAUTION: For External Use Only. Non sterile. Single Use Only. Not Made with Natural Rubber Latex. Store in a Cool, Dry Place. Avoid Direct Sunlight. FDA UDI
Model / Reference
C-NSG228 FDA UDI
Description
Premium Gauze Sponges 2 x 2in. (5.1 x 5.1cm) 8 Ply. Woven 100 percent Cotton. CAUTION: For External Use Only. Non sterile. Single Use Only. Not Made with Natural Rubber Latex. Store in a Cool, Dry Place. Avoid Direct Sunlight. FDA UDI

Identifiers

Catalog Number
C-NSG228 FDA UDI
Primary DI / UDI-DI
20885380052931 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

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Manufacturer

Sources (1)

  • FDA UDI 4ed33f51-0eb8-4b67-9a6e-6d5e8ed694bc 34 fields · synced Jun 8, 2026