FDA UDI In Commercial Distribution 🇺🇸 United States

Medline Industries, Inc.

DI: 10195327429775 · Model: DYNJ58240C · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Medline Industries, Inc.
Primary DI
10195327429775
Version / Model
DYNJ58240C
Catalog Number
DYNJ58240C
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-29
Public Version
1
Public Version Date
2023-08-07
Public Version Status
New
Public Device Record Key
c1163c77-56d8-45b8-98ca-f9a4fcd20a4c

Device Description

HYBRID ARTERIOGRAM

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
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
OEZ Cardiovascular procedure kit

GMDN Terms

Code Name
33961 General surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Package 40195327429776
Primary 10195327429775

Customer Contacts