MVR®

GUDID 20613994931003

BAG MVR1600 RESERVOIR VRB 1600ML 6PK

MEDTRONIC, INC.

Cardiotomy reservoir Cardiotomy reservoir

• Primary Device ID: 20613994931003
• NIH Device Record Key: 6d33d711-278e-4166-8788-d943c3d53e20
• Commercial Distribution Discontinuation: 2017-11-30
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: MVR®
• Version Model Number: MVR1600
• 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: false
• 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	00613994931009 [Primary]
GS1	20613994931003 [Package]; Contains: 00613994931009; Package: PK [6 Units]; Discontinued: 2017-11-30; Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K920774

FDA Product Code

• DTN: RESERVOIR, BLOOD, 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: 4
• Public Version Date: 2020-01-22
• Device Publish Date: 2016-06-16

On-Brand Devices [MVR®]

• 20613994931027: RESERVOIR CBMVR1600 BIOACT STERILE 6PK
• 20613994931010: RESERVOIR CBMVR800 BIOACT STERILE 6PK
• 20613994931003: BAG MVR1600 RESERVOIR VRB 1600ML 6PK
• 20613994930990: BAG MVR800 RESERVOIR VRB 800ML 6PK