FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE

DI: 20193489015994 · Model: NON21430LFPP · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

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Basic Information

Brand Name
MEDLINE
Primary DI
20193489015994
Version / Model
NON21430LFPP
Catalog Number
NON21430LFPP
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2025-06-12
Public Version
1
Public Version Date
2025-06-20
Public Version Status
New
Public Device Record Key
446410a8-77b9-413c-8f03-796f6e7444bc

Device Description

GAUZE,SPONGE,XRAY,4"X4",16PLY,STRL,10/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
GDY Gauze/sponge, internal, x-ray detectable

GMDN Terms

Code Name
38496 Radiopaque woven surgical sponge

Identifiers

Type ID
Package 30193489015991
Primary 20193489015994
Unit of Use 10193489015997

Customer Contacts