Cuff Set, X-Large V23-0001

GUDID 00817980020962

Cuff Set, X-Large

VASOMEDICAL, INC.

External counterpulsation system, stationary

• Primary Device ID: 00817980020962
• NIH Device Record Key: a50f25a2-d5f1-4e6e-ba73-cb71a4aaa988
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cuff Set, X-Large
• Version Model Number: Model Lumenair
• Catalog Number: V23-0001
• Company DUNS: 197210248
• Company Name: VASOMEDICAL, INC.
• 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: false
• Device Combination Product: false
• Single Use: false
• 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(516)508-5818
• Email: eohara@vasomedical.com
• Phone: +1(516)508-5818
• Email: eohara@vasomedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817980020962 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K033617

FDA Product Code

• DRN: Device, counter-pulsating, external

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-11-29

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