FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE

DI: 10197344018482 · Model: 948807146 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
MEDLINE
Primary DI
10197344018482
Version / Model
948807146
Catalog Number
948807146
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-15
Public Version
1
Public Version Date
2023-09-25
Public Version Status
New
Public Device Record Key
77761bb6-4d36-4474-8ddb-2ae5774728ab

Device Description

FDS,72,LARGE,BORE,SPIKE,W/SQZ,CHAMBER

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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FPA Set, administration, intravascular

GMDN Terms

Code Name
58977 Basic intravenous administration set, noninvasive

Identifiers

Type ID
Package 30197344018486
Package 20197344018489
Primary 10197344018482

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K852140 000