BEWELL CONNECT MyOxy

GUDID 03760165448167

VISIOMED GROUP

Pulse oximeter

• Primary Device ID: 03760165448167
• NIH Device Record Key: 0c7b2b9f-3cd0-40fe-8e74-750b61edb97a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BEWELL CONNECT MyOxy
• Version Model Number: BW-OX1
• 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	03760165448167 [Primary]

FDA Product Code

• DQA: Oximeter

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: 2021-11-10
• Device Publish Date: 2017-04-28

Devices Manufactured by VISIOMED GROUP

• 03760165448167 - BEWELL CONNECT MyOxy: 2021-11-10
• 03760165448167 - BEWELL CONNECT MyOxy: 2021-11-10
• 03700609705098 - THERMOFLASH: 2020-12-04
• 03700609705104 - THERMOFLASH: 2020-12-04
• 03700609705111 - THERMOFLASH: 2020-12-04
• 03700609705128 - THERMOFLASH: 2020-12-04
• 03700609705135 - THERMOFLASH: 2020-12-04
• 03700609705142 - THERMOFLASH: 2020-12-04
• 03760165440291 - BEWELL CONNECT MyThermo: 2020-12-04