FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10884389102732 · Model: MDS231318LF · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
Medline
Primary DI
10884389102732
Version / Model
MDS231318LF
Catalog Number
MDS231318LF
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2021-03-31
Public Version
2
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
041fe0d3-f285-4692-9f16-c9b99acf46a0

Device Description

SPONGE,LAP,18"X18",XR,ST,5/TRAY

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
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 40884389102733
Primary 10884389102732
Unit of Use 80884389102731

Customer Contacts