FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 20884389110536 · Model: NON21430CC · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Medline
Primary DI
20884389110536
Version / Model
NON21430CC
Catalog Number
NON21430CC
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2021-04-01
Public Version
2
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
e3b8f412-2045-4a38-ad76-5f3d7df9f61f

Device Description

DBD-GAUZE, CC, 4X4, XR, 16 PLY-NO RETU

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 40884389110530
Primary 20884389110536
Unit of Use 80884389110538

Customer Contacts