FDA UDI In Commercial Distribution 🇺🇸 United States

Curity

DI: 20192253047131 · Model: 6939 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Curity
Primary DI
20192253047131
Version / Model
6939
Catalog Number
6939
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2024-08-02
Public Version
2
Public Version Date
2025-04-18
Public Version Status
Update
Public Device Record Key
ef5a87fe-5ffe-4645-a7b4-048f05a7263b

Device Description

Curity Gauze Sponges

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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FRL FIBER, MEDICAL, ABSORBENT

GMDN Terms

Code Name
48134 Woven gauze pad, non-antimicrobial

Identifiers

Type ID
Package 50192253047132
Primary 20192253047131
Unit of Use 10192253047134

Device Sizes

Type Value Unit Text
Width 4 Inch
Length 4 Inch