Medtronic MiniMed Pro-Set Infusion Set, Luer Connection 42in 328613

GUDID 50382903286138

MINIMED 42IN LUER MMT-291600

Becton, Dickinson and Company Inc

Electric infusion pump administration set, single-use
Primary Device ID50382903286138
NIH Device Record Key98508317-b8a0-4e30-9091-8d132b344521
Commercial Distribution StatusIn Commercial Distribution
Brand NameMedtronic MiniMed Pro-Set Infusion Set, Luer Connection 42in
Version Model Number328613
Catalog Number328613
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

Length42 Inch
Length42 Inch
Length42 Inch
Length42 Inch
Length42 Inch
Length42 Inch
Length42 Inch
Length42 Inch
Length42 Inch
Length42 Inch
Length42 Inch
Length42 Inch
Length42 Inch
Length42 Inch
Length42 Inch
Length42 Inch
Length42 Inch
Length42 Inch
Length42 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100382903286133 [Primary]
GS100382903672974 [Unit of Use]
GS150382903286138 [Package]
Contains: 00382903286133
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 42in]

50382903286138MINIMED 42IN LUER MMT-291600
50382903286114MINIMED 42IN LUER MMT-291

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