LVIS 213015-LVIS

GUDID 00842429100943

Stent

MICROVENTION INC.

Bare-metal intracranial vascular stent

• Primary Device ID: 00842429100943
• NIH Device Record Key: 422aa4cf-e372-4617-a102-6e65d564a9dc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LVIS
• Version Model Number: 213015-LVIS-D-PMA
• Catalog Number: 213015-LVIS
• Company DUNS: 003263105
• Company Name: MICROVENTION INC.
• Device Count: 1
• DM Exempt: true
• 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: (714) 247-8000
• Email: customerservice@microvention.com
• Phone: (714) 247-8000
• Email: customerservice@microvention.com
• Phone: (714) 247-8000
• Email: customerservice@microvention.com
• Phone: (714) 247-8000
• Email: customerservice@microvention.com
• Phone: (714) 247-8000
• Email: customerservice@microvention.com
• Phone: (714) 247-8000
• Email: customerservice@microvention.com
• Phone: (714) 247-8000
• Email: customerservice@microvention.com
• Phone: (714) 247-8000
• Email: customerservice@microvention.com
• Phone: (714) 247-8000
• Email: customerservice@microvention.com
• Phone: (714) 247-8000
• Email: customerservice@microvention.com
• Phone: (714) 247-8000
• Email: customerservice@microvention.com
• Phone: (714) 247-8000
• Email: customerservice@microvention.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00842429100943 [Primary]

FDA Product Code

• QCA: Intracranial Coil-Assist Stent

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-07-27
• Device Publish Date: 2018-06-26

On-Brand Devices [LVIS]

• 00810170019043: Stent
• 00810170019036: Stent
• 00810170019029: Stent
• 00810170019012: Stent
• 00810170019005: Stent
• 00810170018626: Stent
• 00810170018619: Stent
• 00810170016349: Stent
• 00810170016332: Stent
• 00810170016325: Stent
• 00810170016318: Stent
• 00810170016301: Stent
• 00810170016295: Stent
• 00810170016288: Stent
• 00812636022246: Stent
• 00812636022239: Stent
• 00812636022222: Stent
• 00812636022215: Stent
• 00812636022208: Stent
• 00812636022192: Stent
• 00812636022185: Stent
• 00811425029992: Stent
• 00811425029985: Low-Profile Visualized Intraluminal Support
• 00811425029978: Low-Profile Visualized Intraluminal Support
• 00811425029961: Low-Profile Visualized Intraluminal Support
• 00811425029954: Low-Profile Visualized Intraluminal Support
• 00811425029947: Low-Profile Visualized Intraluminal Support
• 00811425029930: Low-Profile Visualized Intraluminal Support
• 00816777026026: Stent
• 00816777026019: Stent
• 00816777026002: Stent
• 00816777025999: Stent
• 00816777025982: Stent
• 00842429100981: Stent
• 00842429100974: Stent
• 00842429100967: Stent
• 00842429100950: Stent
• 00842429100943: Stent
• 00842429100936: Stent
• 00842429100929: Stent
• 00842429100912: Stent
• 00842429100905: Stent
• 00842429100899: Stent
• 00842429100882: Stent
• 00842429100875: Stent