BEWELL CONNECT MyTensio

GUDID 03760165440932

VISIOMED GROUP

Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

• Primary Device ID: 03760165440932
• NIH Device Record Key: 0a7b8842-c46c-45d0-a24a-735f502dbe29
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BEWELL CONNECT MyTensio
• Version Model Number: BW-BA1
• Company DUNS: 261118805
• Company Name: VISIOMED GROUP
• 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: true
• Manufacturing Date: true
• 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	03760165440932 [Primary]

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: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-11-08
• Device Publish Date: 2017-04-28

On-Brand Devices [BEWELL CONNECT MyTensio]

• 03760165449287: BW-BW1
• 03760165440932: BW-BA1