WEB W5-5-3

GUDID 00842429110850

WEB 17 SL 5x3

MICROVENTION INC.

Neurovascular embolization coil

• Primary Device ID: 00842429110850
• NIH Device Record Key: 27a29228-90f4-4022-ae27-2090bffd7913
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WEB
• Version Model Number: W5-5-3-MVI-3
• Catalog Number: W5-5-3
• 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: true
• 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

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 Identifiers

Device Issuing Agency	Device ID
GS1	00842429110850 [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: 2021-06-08
• Device Publish Date: 2021-05-31

On-Brand Devices [WEB]

• 00842429110966: WEB 17 SLS 7
• 00842429110959: WEB 17 SL 7x6
• 00842429110942: WEB 17 SL 7x5
• 00842429110935: WEB 17 SL 7x4
• 00842429110928: WEB 17 SL 7x3
• 00842429110911: WEB 17 SLS 6
• 00842429110904: WEB 17 SL 6x5
• 00842429110898: WEB 17 SL 6x4
• 00842429110881: WEB 17 SL 6x3
• 00842429110874: WEB 17 SLS 5
• 00842429110867: WEB 17 SL 5x4
• 00842429110850: WEB 17 SL 5x3
• 00842429110843: WEB 17 SL 5x2
• 00842429110836: WEB 17 SLS 4
• 00842429110829: WEB 17 SL 4x3
• 00842429110812: WEB 17 SL 4x2
• 00842429110805: WEB 17 SL 4.5x3
• 00842429110799: WEB 17 SL 4.5x2