WEB 17 SL 7x2 W5-7-2

GUDID 00842429118009

WEB Aneurysm Embolization System

MICROVENTION INC.

Neurovascular embolization coil

• Primary Device ID: 00842429118009
• NIH Device Record Key: d50ea29d-2124-4ffa-95b4-9c5a46811a7b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WEB 17 SL 7x2
• Version Model Number: W5-7-2-MVI-3
• Catalog Number: W5-7-2
• Company DUNS: 003263105
• Company Name: MICROVENTION INC.
• 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: true
• Expiration Date: true
• 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(714) 247-8000
• Email: customerservice@microvention.com
• Phone: +1(714) 247-8000
• Email: customerservice@microvention.com
• Phone: +1(714) 247-8000
• Email: customerservice@microvention.com
• Phone: +1(714) 247-8000
• Email: customerservice@microvention.com
• Phone: +1(714) 247-8000
• Email: customerservice@microvention.com
• Phone: +1(714) 247-8000
• Email: customerservice@microvention.com
• Phone: +1(714) 247-8000
• Email: customerservice@microvention.com
• Phone: +1(714) 247-8000
• Email: customerservice@microvention.com
• Phone: +1(714) 247-8000
• Email: customerservice@microvention.com
• Phone: +1(714) 247-8000
• Email: customerservice@microvention.com
• Phone: +1(714) 247-8000
• Email: customerservice@microvention.com
• Phone: +1(714) 247-8000
• Email: customerservice@microvention.com
• Phone: +1(714) 247-8000
• Email: customerservice@microvention.com
• Phone: +1(714) 247-8000
• Email: customerservice@microvention.com
• Phone: +1(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 Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00842429118009 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P170032

FDA Product Code

• OPR: Intrasaccular Flow Disruption Device

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: 2023-05-04
• Device Publish Date: 2023-04-26

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• 00842429118795 - AZUR Detachment Controller: 2025-09-09 AZUR Detachment Controller
• 00816777020116 - V-Grip Detachment Controller: 2025-09-05 V-Grip Detachment Controller
• 00840273201991 - AZUR Detachment Controller: 2025-09-05 AZUR Detachment Controller
• 00840273202028 - V-Grip Detachment Controller: 2025-09-05 V-Grip Detachment Controller
• 00842429106464 - V-Grip Detachment Controller: 2025-09-05 V-Grip Detachment Controller
• 00811425020852 - Roadsaver Carotid Atery Stent: 2025-08-11 Roadsaver Carotid Atery Stent