1-FEMORAL CATHETER KIT (5F, 20 CM), SINGLE PACK VLVFC520

GUDID 00690103190397

VolumeView

Edwards Lifesciences LLC

Peripheral vascular catheter

• Primary Device ID: 00690103190397
• NIH Device Record Key: b8bfb535-f2ac-4a04-8b55-15589d029a10
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 1-FEMORAL CATHETER KIT (5F, 20 CM), SINGLE PACK
• Version Model Number: VLVFC520
• Catalog Number: VLVFC520
• 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
• Device Kit: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)822-9637
• Email: tech_support@edwards.com
• Phone: +1(800)822-9637
• 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	00690103190397 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K100739

FDA Product Code

• KRB: PROBE, THERMODILUTION

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: 2016-09-03

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