RENPHO Blood Pressure Monitor

GUDID 10810140060980

Joicom Corporation

Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

• Primary Device ID: 10810140060980
• NIH Device Record Key: e0c8b20a-33e4-49cf-9a68-3bf347b431de
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RENPHO Blood Pressure Monitor
• Version Model Number: RP-BPM001S
• Company DUNS: 033774836
• 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: false
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810140060983 [Primary]
GS1	10810140060980 [Package]; Contains: 00810140060983; Package: case [40 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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-02-17
• Device Publish Date: 2023-08-08

On-Brand Devices [RENPHO Blood Pressure Monitor]

• 10860002249640: RP-BPM003
• 00860002249681: RP-BPM004
• 04897106770045: RP-BPM001S
• 10850023727012: RP-BPM001S
• 10850023727029: RP-BPM001
• 10810140060980: RP-BPM001S
• 10810140060973: RP-BPM001