Chaperon Guiding Catheter GC595BUST

GUDID 00810170013218

Guides

MICROVENTION INC.

Vascular guide-catheter, single-use

• Primary Device ID: 00810170013218
• NIH Device Record Key: e3278bc2-0b93-4df0-a5ac-24c427111ed4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Chaperon Guiding Catheter
• Version Model Number: GC595BUST
• Catalog Number: GC595BUST
• 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: +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
• 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
• 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 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	00810170013218 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K082385

FDA Product Code

• DQY: CATHETER, PERCUTANEOUS

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-01-23
• Device Publish Date: 2016-09-24

On-Brand Devices [Chaperon Guiding Catheter]

• 00810170013379: Guides
• 00810170013362: Guides
• 00810170013355: Guides
• 00810170013348: Guides
• 00810170013331: Guides
• 00810170013324: Guides
• 00810170013317: Guides
• 00810170013300: Guides
• 00810170013294: Guides
• 00810170013287: Guides
• 00810170013270: Guides
• 00810170013263: Guides
• 00810170013256: Guides
• 00810170013249: Guides
• 00810170013232: Guides
• 00810170013225: Guides
• 00810170013218: Guides
• 00810170013201: Guides
• 00810170013195: Guides
• 00810170013188: Guides
• 00810170013171: Guides
• 00810170013164: Guides
• 00810170013157: Guides
• 00810170013140: Guides
• 00810170013133: Guides
• 00810170012877: Guides
• 00810170012860: Guides
• 00810170012853: Guides
• 00810170012846: Guides
• 00810170012839: Guides
• 00810170012822: Guides
• 00810170012815: Guides
• 00810170012808: Guides
• 00810170012433: Guides
• 00810170012426: Guides
• 00810170012419: Guides
• 00810170012402: Guides
• 00810170012396: Guides
• 00810170012389: Guides
• 00810170012372: Guides
• 00810170012365: Guides
• 00810170012358: Guides
• 00810170012341: Guides
• 00810170012334: Guides
• 00810170012327: Guides
• 00810170012310: Guides
• 00810170012303: Guides
• 00810170012297: Guides