RENPHO BLOOD PRESSURE MONITOR RP-BPM003

GUDID 10860002249640

JOICOM CORPORATION

Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

• Primary Device ID: 10860002249640
• NIH Device Record Key: 9e25f183-8b3b-4cd1-a858-f21bd2763339
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RENPHO BLOOD PRESSURE MONITOR
• Version Model Number: RP-BPM003
• Catalog Number: RP-BPM003
• Company DUNS: 081060692
• Company Name: JOICOM CORPORATION
• 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	00860002249643 [Primary]
GS1	10860002249640 [Package]; Contains: 00860002249643; Package: [12 Units]; In Commercial Distribution

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: 2020-04-13
• Device Publish Date: 2020-04-03

On-Brand Devices [RENPHO BLOOD PRESSURE MONITOR]

• 10860002249640: RP-BPM003
• 00860002249681: RP-BPM004
• 04897106770045: RP-BPM001S
• 10850023727012: RP-BPM001S
• 10850023727029: RP-BPM001