Minimax Plus®

GUDID 30673978546194

OXYGENATOR 3381 MINIMAX PLUS STAND 4PK

MEDTRONIC, INC.

Extracorporeal membrane oxygenator Extracorporeal membrane oxygenator

• Primary Device ID: 30673978546194
• NIH Device Record Key: fbfdda42-b592-4115-af4e-5556fc250791
• Commercial Distribution Discontinuation: 2018-10-05
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Minimax Plus®
• Version Model Number: 3381
• Company DUNS: 006261481
• Company Name: MEDTRONIC, INC.
• Device Count: 1
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00673978546193 [Primary]
GS1	30673978546194 [Package]; Contains: 00673978546193; Package: PK [4 Units]; Discontinued: 2018-10-05; Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K933586

FDA Product Code

• FRL: FIBER, MEDICAL, ABSORBENT

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2020-01-22
• Device Publish Date: 2015-06-09

On-Brand Devices [Minimax Plus®]

• 20613994269779: OXY 3301 MINIMAX PLUS W/HARDSHELL 2PK
• 30673978546194: OXYGENATOR 3381 MINIMAX PLUS STAND 4PK