FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE

DI: 10193489109733 · Model: 6010156441 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
MEDLINE
Primary DI
10193489109733
Version / Model
6010156441
Catalog Number
6010156441
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
90a40bfb-ab7b-48ec-8c7e-691ce47eaef1

Device Description

PSP,AKRON GENERAL HEALTH SYSTEM

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 20193489109730
Primary 10193489109733
Package 30193489109737

Customer Contacts