FDA UDI In Commercial Distribution 🇺🇸 United States

Medline Industries, Inc.

DI: 10193489759303 · Model: DYNJ0376230Q · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Medline Industries, Inc.
Primary DI
10193489759303
Version / Model
DYNJ0376230Q
Catalog Number
DYNJ0376230Q
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-08-04
Public Version
5
Public Version Date
2023-07-27
Public Version Status
Update
Public Device Record Key
2669e372-ffd2-4d8a-bec2-edaeb01efb7b

Device Description

INTERVENTIONAL CATH LAB PK-LF

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
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 10193489759303
Package 40193489759304

Customer Contacts