Minimax®

GUDID 20613994269786

RSVR 1316 MINIMAX INF STD ALN HRDSHL 4PK

MEDTRONIC, INC.

Cardiotomy reservoir

• Primary Device ID: 20613994269786
• NIH Device Record Key: 90a2e8be-4708-4574-88d0-67b9309bf1de
• Commercial Distribution Discontinuation: 2018-10-05
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Minimax®
• Version Model Number: 1316
• 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	00613994269782 [Primary]
GS1	20613994269786 [Package]; Contains: 00613994269782; Package: PK [4 Units]; Discontinued: 2018-10-05; Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K911789

FDA Product Code

• DTP: Defoamer, cardiopulmonary bypass

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®]

• 20613994269786: RSVR 1316 MINIMAX INF STD ALN HRDSHL 4PK
• 20613994965138: OXYGENATOR CB3381 BIOACT MINIMAX S 4PKL