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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
Radiopaque woven surgical sponge, non-sterile FDA UDI
Device Name
Cardinal Health Lap Sponge 12 X 12 in. Unwashed X-Ray Detectable Softpack FDA UDI
Model / Reference
23250-409 FDA UDI
Description
Cardinal Health Lap Sponge 12 X 12 in. Unwashed X-Ray Detectable Softpack FDA UDI

Identifiers

Catalog Number
23250-409 FDA UDI
Primary DI / UDI-DI
30885380121719 FDA UDI
FDA Product Code
GDY FDA UDI
GMDN Term
Radiopaque woven surgical sponge, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4450 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Dimensions & Sizes

Size
Length — 12 Inch FDA UDI
Height — 12 Inch FDA UDI

Category: Radiopaque woven surgical sponge, 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 Radiopaque woven surgical sponge, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinal Health 200, LLC

Sources (1)

  • FDA UDI d157cabd-027c-4db2-836b-0425adf8ce4d 35 fields · synced Jun 6, 2026