FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE

DI: 10889942926985 · Model: DYNJSC4HPFF · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MEDLINE
Primary DI
10889942926985
Version / Model
DYNJSC4HPFF
Catalog Number
DYNJSC4HPFF
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-08-12
Public Version
1
Public Version Date
2025-08-20
Public Version Status
New
Public Device Record Key
7a0066a6-1a83-4e76-8421-fe9609df0731

Device Description

STOPCOCK,4-WAY,HIGH FLOW,OFF,SWIVEL

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
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
No
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
35375 Stopcock

Identifiers

Type ID
Package 40889942926986
Primary 10889942926985

Customer Contacts