23MM X 29MM X 55CM ASCENDRA+ DELIVERY SYSTEM 9355AS23A

GUDID 00690103193718

23MM ASCENDRA+ DELIVERY SYSTEM

Edwards Lifesciences LLC

Cardiac valvuloplasty catheter

• Primary Device ID: 00690103193718
• NIH Device Record Key: 5de7e841-2c07-4ead-a4b9-7aee88699fd9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 23MM X 29MM X 55CM ASCENDRA+ DELIVERY SYSTEM
• Version Model Number: 9355AS23
• Catalog Number: 9355AS23A
• Company DUNS: 134139174
• Company Name: Edwards Lifesciences LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)822-9837
• Email: tech_support@edwards.com
• Phone: +1(800)822-9837
• Email: tech_support@edwards.com

Device Dimensions

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00690103193718 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P130009

FDA Product Code

• NPT: Aortic valve, prosthesis, percutaneously delivered

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2014-08-30

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• 57460691947462 - TRUWAVE, VAMP: 2024-09-12 PRESSURE MONITORING SET
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