FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE INDUSTRIES, INC.

DI: 10198459421785 · Model: DYNJ50739J · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MEDLINE INDUSTRIES, INC.
Primary DI
10198459421785
Version / Model
DYNJ50739J
Catalog Number
DYNJ50739J
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-07-21
Public Version
1
Public Version Date
2025-07-29
Public Version Status
New
Public Device Record Key
b4da5a5f-7744-4930-8a31-92760035d8b4

Device Description

ANGIO PACK

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
OES Cardiac catheterization kit

GMDN Terms

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

Identifiers

Type ID
Package 40198459421786
Primary 10198459421785

Customer Contacts