FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE

DI: 10193489099423 · Model: 6010236231 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
MEDLINE
Primary DI
10193489099423
Version / Model
6010236231
Catalog Number
6010236231
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-15
Public Version
1
Public Version Date
2023-09-25
Public Version Status
New
Public Device Record Key
d4cc40b0-4f1a-4fdf-ae94-c9024b5ee603

Device Description

MTS,LHK,UTMB,AT,GALVESTON

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
Yes
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OEZ Cardiovascular procedure kit

GMDN Terms

Code Name
16545 Angiography kit

Identifiers

Type ID
Package 20193489099420
Primary 10193489099423
Package 30193489099427

Customer Contacts