3 Series Blood Pressure Monitor BP710CANN

GUDID 00073796710347

Omron Blood Pressure Monitor, 3 Series

Omron Healthcare, Inc.

Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

• Primary Device ID: 00073796710347
• NIH Device Record Key: 4eee8f16-5e5e-43bb-9e20-d7bff7c5e000
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 3 Series Blood Pressure Monitor
• Version Model Number: BP710CANN
• Catalog Number: BP710CANN
• Company DUNS: 054318779
• Company Name: Omron Healthcare, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• 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: true

Customer Support Contacts

• Phone: 1-800-634-4350
• Email: quality@omron.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00073796710347 [Primary]
GS1	10073796710344 [Package]; Package: Case [12 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K133379

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: 4
• Public Version Date: 2019-11-08
• Device Publish Date: 2016-09-16

On-Brand Devices [3 Series Blood Pressure Monitor]

• 00073796710347: Omron Blood Pressure Monitor, 3 Series
• 00073796271046: Blood Pressure Monitor - upper arm