16F X 36CM EDWARDS EXPANDABLE INTRODUCER SHEATH SET 916ES23A

GUDID 00690103192100

EDWARDS EXPANDABLE INTRODUCER SHEATH SET

Edwards Lifesciences LLC

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• Primary Device ID: 00690103192100
• NIH Device Record Key: b58b7533-8890-4d0b-ab09-d4c40ef9164c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 16F X 36CM EDWARDS EXPANDABLE INTRODUCER SHEATH SET
• Version Model Number: 916ES23
• Catalog Number: 916ES23A
• 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
• Phone: +1(800)822-9837
• Email: tech_support@edwards.com
• Phone: +1(800)822-9837
• Email: tech_support@edwards.com
• Phone: +1(800)822-9837
• Email: tech_support@edwards.com
• Phone: +1(800)822-9837
• Email: tech_support@edwards.com
• Phone: +1(800)822-9837
• Email: tech_support@edwards.com
• Phone: +1(800)822-9837
• Email: tech_support@edwards.com
• Phone: +1(800)822-9837
• Email: tech_support@edwards.com
• Phone: +1(800)822-9837
• Email: tech_support@edwards.com
• Phone: +1(800)822-9837
• Email: tech_support@edwards.com
• Phone: +1(800)822-9837
• Email: tech_support@edwards.com
• Phone: +1(800)822-9837
• Email: tech_support@edwards.com
• Phone: +1(800)822-9837
• Email: tech_support@edwards.com
• Phone: +1(800)822-9837
• Email: tech_support@edwards.com
• Phone: +1(800)822-9837
• Email: tech_support@edwards.com
• Phone: +1(800)822-9837
• Email: tech_support@edwards.com
• 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 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	00690103192100 [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: 4
• Public Version Date: 2019-06-07
• Device Publish Date: 2014-08-30

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• 00690103218848 - HemoSphere Vita: 2024-03-05 VitaWave Module
• 00690103218855 - HemoSphere Vita: 2024-03-05 HemoSphere Vita Monitor
• 00690103218862 - HemoSphere Vita: 2024-03-05 Vita Technology Module
• 50690103218898 - VitaWave: 2024-02-28 VitaWave Finger Cuff Adult
• 00690103217483 - EVOQUE: 2024-02-15 Edwards EVOQUE Stabilizer Plate
• 00690103217490 - EVOQUE: 2024-02-15 Edwards EVOQUE Loading System
• 00690103217506 - EVOQUE: 2024-02-15 Edwards EVOQUE Dilator Kit (24, 28, 33 Fr dilators)