BEWELL CONNECT MyOxy

GUDID 03760165448167

VISIOMED GROUP

Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter 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