TupeloLife

GUDID 10860005787200

Tupelolife Services LLC

Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

• Primary Device ID: 10860005787200
• NIH Device Record Key: 688d706c-8528-49f1-a95d-2259737582cb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TupeloLife
• Version Model Number: TBP-001
• Company DUNS: 080844144
• Company Name: Tupelolife Services 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: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860005787203 [Primary]
GS1	10860005787200 [Package]; Contains: 00860005787203; Package: carton [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K123780

FDA Product Code

• DXN: System, Measurement, Blood-Pressure, Non-Invasive

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-12-04
• Device Publish Date: 2020-11-26

On-Brand Devices [TupeloLife]

• 10860005787200: TBP-001
• 10860005787217: TBP-002