FDA UDI In Commercial Distribution 🇺🇸 United States

MEDICAL ACTION INDUSTRIES

DI: 10809160431849 · Model: 44258A-TEST · MEDICAL ACTION INDUSTRIES INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
MEDICAL ACTION INDUSTRIES
Primary DI
10809160431849
Version / Model
44258A-TEST
Company Name
MEDICAL ACTION INDUSTRIES INC.
Labeler DUNS
092364462
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-06
Public Version
2
Public Version Date
2025-04-18
Public Version Status
Update
Public Device Record Key
cdf59437-90f0-458c-b189-1d7850b37c6a

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
Yes
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
NAB Gauze / sponge,nonresorbable for external use

GMDN Terms

Code Name
48134 Woven gauze pad, non-antimicrobial

Identifiers

Type ID
Package 20809160431846
Primary 10809160431849
Package 30809160431843