Medtronic MiniMed Pro-Set Infusion Set, Luer Connection 24in 328610

GUDID 50382903286107

MINIMED 24IN LUER MMT-290

Becton, Dickinson and Company Inc

Electric infusion pump administration set, single-use
Primary Device ID50382903286107
NIH Device Record Keye43f2309-5498-4703-a778-f06b7aeeea78
Commercial Distribution StatusIn Commercial Distribution
Brand NameMedtronic MiniMed Pro-Set Infusion Set, Luer Connection 24in
Version Model Number328610
Catalog Number328610
Company DUNS047047543
Company NameBecton, Dickinson and Company Inc
Device Count150
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Dimensions

Length24 Inch
Length24 Inch
Length24 Inch
Length24 Inch
Length24 Inch
Length24 Inch
Length24 Inch
Length24 Inch
Length24 Inch
Length24 Inch
Length24 Inch
Length24 Inch
Length24 Inch
Length24 Inch
Length24 Inch
Length24 Inch
Length24 Inch
Length24 Inch
Length24 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100382903286102 [Primary]
GS100382903672929 [Unit of Use]
GS150382903286107 [Package]
Contains: 00382903286102
Package: Case [15 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FPASet, administration, intravascular

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-08-03

On-Brand Devices [Medtronic MiniMed Pro-Set Infusion Set, Luer Connection 24in]

00382903286126MINIMED 24IN LUER MMT-290600
50382903286107MINIMED 24IN LUER MMT-290

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.