FDA UDI In Commercial Distribution 🇺🇸 United States

Medline Industries, Inc.

DI: 10193489787702 · Model: DYNJ59315A · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Medline Industries, Inc.
Primary DI
10193489787702
Version / Model
DYNJ59315A
Catalog Number
DYNJ59315A
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-09-09
Public Version
5
Public Version Date
2023-07-27
Public Version Status
Update
Public Device Record Key
53f2fdc5-0958-4367-a171-bd95e8a3708d

Device Description

STANDARD CATH PACK

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
No
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OEQ Angiography/angioplasty kit

GMDN Terms

Code Name
44057 General surgical procedure kit, medicated

Identifiers

Type ID
Primary 10193489787702
Package 40193489787703

Customer Contacts