FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE

DI: 20080196692900 · Model: NON25852 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
2

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
MEDLINE
Primary DI
20080196692900
Version / Model
NON25852
Catalog Number
NON25852
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
5943e8e2-e9ed-4fa2-8a28-70ee14281aae

Device Description

GAUZE,SPONGE,FLUFF,6"X6.75",STRL,2'S

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
48134 Woven gauze pad, non-antimicrobial

Identifiers

Type ID
Package 40080196692904
Primary 20080196692900
Package 30080196692907
Unit of Use 10080196692903

Customer Contacts