FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE

DI: 20080196690807 · Model: NON21442 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
2

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Basic Information

Brand Name
MEDLINE
Primary DI
20080196690807
Version / Model
NON21442
Catalog Number
NON21442
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2025-06-02
Public Version
1
Public Version Date
2025-06-10
Public Version Status
New
Public Device Record Key
b8d1386c-fa4e-4a9a-a562-f6e1a41d78ca

Device Description

GAUZE,SPONGE,POST-OP,4X4,STRL,LF,2/PK

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
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
No
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
48131 Non-woven gauze pad

Identifiers

Type ID
Package 40080196690801
Primary 20080196690807
Package 30080196690804
Unit of Use 10080196690800

Customer Contacts