CARDINAL HEALTH

Basic Information

• Brand Name: CARDINAL HEALTH
• Primary DI: 20885380053372
• Version / Model: C-NXR4832
• Catalog Number: C-NXR4832
• Company Name: Cardinal Health 200, LLC
• Labeler DUNS: 961027315
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 100
• Record Status: Published
• Publish Date: 2019-06-19
• Public Version: 1
• Public Version Date: 2019-06-27
• Public Version Status: New
• Public Device Record Key: a7dd11de-64bb-48b2-a2c9-5b121b9780f0

Device Description

X-Ray Detectable Sponges / 4 x 8in. (10.2 x 20.3cm) CAUTION: For External Use Only. 32-Ply Woven 100 percent Cotton with Wavy Barium Sulfate Band. Non Sterile. Single Use Only. Not Made with Natural Rubber Latex. Store in a Cool, Dry Place.

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): No
• Over the Counter (OTC): Yes
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: Yes
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: Yes
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
NAB	Gauze / sponge,nonresorbable for external use	General, Plastic Surgery	878.4014	1

GMDN Terms

Code	Name	Definition	Implantable	Status
58802	Radiopaque woven surgical sponge, non-sterile	A non-medicated non-sterile device made from woven gauze (e.g., cotton, cellulose) primarily intended to be used inside the body, on a surgical incision or applied to internal organs or structures to control bleeding, absorb fluid, or protect organs or structures from abrasion, drying, or contamination during a procedure; also referred to as a laparotomy sponge, it may also be used for prepping the patient. It contains an x-ray detectable marker [e.g., a thread or strand(s)] to help detect gossypiboma (sponge left inside patient). This is a single-use device intended to be sterilized prior to use.	No	Obsolete

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Package	50885380053373	GS1	CASE	10	In Commercial Distribution
Primary	20885380053372	GS1
Unit of Use	00885380053378	GS1