Blood Pressure Cuff

GUDID 00815871022552

THIGH SINGLE LUMEN 41-54CM

Avante

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• Primary Device ID: 00815871022552
• NIH Device Record Key: 7a17a9ae-ce93-424b-8a2b-d2c71e0b023e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Blood Pressure Cuff
• Version Model Number: 80031-T
• Company DUNS: 178440426
• Company Name: Avante
• 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: true
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 502-244-4444
• Email: DeviceHelp@dremed.com
• Phone: 502-244-4444
• Email: DeviceHelp@dremed.com
• Phone: 502-244-4444
• Email: DeviceHelp@dremed.com
• Phone: 502-244-4444
• Email: DeviceHelp@dremed.com
• Phone: 502-244-4444
• Email: DeviceHelp@dremed.com
• Phone: 502-244-4444
• Email: DeviceHelp@dremed.com
• Phone: 502-244-4444
• Email: DeviceHelp@dremed.com
• Phone: 502-244-4444
• Email: DeviceHelp@dremed.com
• Phone: 502-244-4444
• Email: DeviceHelp@dremed.com
• Phone: 502-244-4444
• Email: DeviceHelp@dremed.com
• Phone: 502-244-4444
• Email: DeviceHelp@dremed.com
• Phone: 502-244-4444
• Email: DeviceHelp@dremed.com
• Phone: 502-244-4444
• Email: DeviceHelp@dremed.com
• Phone: 502-244-4444
• Email: DeviceHelp@dremed.com
• Phone: 502-244-4444
• Email: DeviceHelp@dremed.com
• Phone: 502-244-4444
• Email: DeviceHelp@dremed.com
• Phone: 502-244-4444
• Email: DeviceHelp@dremed.com
• Phone: 502-244-4444
• Email: DeviceHelp@dremed.com
• Phone: 502-244-4444
• Email: DeviceHelp@dremed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00815871022552 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K143728

FDA Product Code

• DXQ: Blood Pressure Cuff

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-07-22
• Device Publish Date: 2017-05-26

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