FDA UDI In Commercial Distribution 🇺🇸 United States

Curity

DI: 20192253049494 · Model: 8042 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
2

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Basic Information

Brand Name
Curity
Primary DI
20192253049494
Version / Model
8042
Catalog Number
8042
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
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
cdc25a1a-95a1-4fb6-80b7-8361eeb6fb90

Device Description

Curity All Purpose 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
No
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 50192253049495
Package 30192253049491
Primary 20192253049494
Unit of Use 10192253049497

Device Sizes

Type Value Unit Text
Length 2 Inch
Width 2 Inch