FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE

DI: 10193489068122 · Model: 85000936 · MEDLINE INDUSTRIES, INC.
Product Codes
3
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
MEDLINE
Primary DI
10193489068122
Version / Model
85000936
Catalog Number
85000936
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-18
Public Version
1
Public Version Date
2023-09-26
Public Version Status
New
Public Device Record Key
4b86bcba-fda9-4c1a-9bf7-72d62402ece0

Device Description

PROT.STA.C.D.S.,DU.CK,VA-SAC,W/ADAP

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
No
Sterilization Prior Use
No

Product Codes

Code Name
DQO Catheter, intravascular, diagnostic
KGZ ACCESSORIES, CATHETER
DTL Adaptor, stopcock, manifold, fitting, cardiopulmonary bypass

GMDN Terms

Code Name
58977 Basic intravenous administration set, noninvasive

Identifiers

Type ID
Package 20193489068129
Primary 10193489068122
Package 30193489068126

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K843726 000
K884408 000
K896087 000