MVP®

GUDID 00847536025431

VASCULAR PLUG MVP-7Q MECHANICAL 7MM V03

Reverse Medical Corporation

Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil Non-neurovascular embolization coil

• Primary Device ID: 00847536025431
• NIH Device Record Key: 6b2ff95f-1a28-4b4a-9c4d-b22359f4eba9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MVP®
• Version Model Number: MVP-7Q
• Company DUNS: 963324913
• Company Name: Reverse Medical Corporation
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• 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	00847536025431 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K150108

FDA Product Code

• KRD: Device, Vascular, for Promoting Embolization

Sterilization

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

[00847536025431]

Ethylene Oxide

[00847536025431]

Ethylene Oxide

[00847536025431]

Ethylene Oxide

[00847536025431]

Ethylene Oxide

[00847536025431]

Ethylene Oxide

[00847536025431]

Ethylene Oxide

[00847536025431]

Ethylene Oxide

[00847536025431]

Ethylene Oxide

[00847536025431]

Ethylene Oxide

[00847536025431]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-06-17
• Device Publish Date: 2016-07-25

On-Brand Devices [MVP®]

• 00847536027732: MICRO VASCULAR PLUG MVP-9Q V03 US EU
• 00847536025431: VASCULAR PLUG MVP-7Q MECHANICAL 7MM V03
• 00847536020832: MICRO VASCULAR PLUG MVP-9Q V02 US
• 00847536004351: MVP-5Q MICRO VASCULAR PLUG
• 00847536004344: MVP-3Q MICRO VASCULAR PLUG
• 00847536004009: MVP-9Q MICRO VASCULAR PLUG
• 00847536003637: PLUG MICRO VASCULAR MVP-7Q
• 00847536003620: MVP-5Q MICRO VASCULAR PLUG
• 00847536003613: MVP-3Q MICRO VASCULAR PLUG
• 00847536003606: MVP-5US MICRO VASCULAR PLUG
• 00847536003583: MVP-3US MICRO VASCULAR PLUG
• 00847536020825: VASCULAR PLUG MVP-7Q MECHANICAL 7MM V02