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 Electric infusion pump administration set, single-use

• Primary Device ID: 50382903286138
• NIH Device Record Key: 98508317-b8a0-4e30-9091-8d132b344521
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medtronic MiniMed Pro-Set Infusion Set, Luer Connection 42in
• Version Model Number: 328613
• Catalog Number: 328613
• Company DUNS: 047047543
• Company Name: Becton, Dickinson and Company Inc
• Device Count: 150
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Dimensions

• Length: 42 Inch
• Length: 42 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00382903286133 [Primary]
GS1	00382903672974 [Unit of Use]
GS1	50382903286138 [Package]; Contains: 00382903286133; Package: Case [15 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K160651

FDA Product Code

• FPA: Set, administration, intravascular

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-08-03

On-Brand Devices [Medtronic MiniMed Pro-Set Infusion Set, Luer Connection 42in]

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