VIA Microcatheter VIA-21-154-01

GUDID 00842429106419

VIA 21 Microcatheter

MICROVENTION INC.

Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter

• Primary Device ID: 00842429106419
• NIH Device Record Key: ba7472ef-3ced-435d-807f-809b6ad1f7fa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VIA Microcatheter
• Version Model Number: VIA-21-154-01-MVI2
• Catalog Number: VIA-21-154-01
• Company DUNS: 003263105
• Company Name: MICROVENTION INC.
• Device Count: 1
• DM Exempt: true
• 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: 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

Device Dimensions

• Lumen/Inner Diameter: 0.021 Inch
• Lumen/Inner Diameter: 0.021 Inch
• Lumen/Inner Diameter: 0.021 Inch
• Lumen/Inner Diameter: 0.021 Inch
• Lumen/Inner Diameter: 0.021 Inch
• Lumen/Inner Diameter: 0.021 Inch
• Lumen/Inner Diameter: 0.021 Inch
• Lumen/Inner Diameter: 0.021 Inch
• Lumen/Inner Diameter: 0.021 Inch
• Lumen/Inner Diameter: 0.021 Inch
• Lumen/Inner Diameter: 0.021 Inch
• Lumen/Inner Diameter: 0.021 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00842429106419 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K192135

FDA Product Code

• DQY: Catheter, percutaneous

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: 2020-09-07
• Device Publish Date: 2020-08-30

On-Brand Devices [VIA Microcatheter]

• 00842429106457: VIA 17 Microcatheter
• 00842429106440: VIA 17 Microcatheter
• 00842429106433: VIA 33 Microcatheter
• 00842429106426: VIA 27 Microcatheter
• 00842429106419: VIA 21 Microcatheter
• 00842429106402: VIA 17 Microcatheter