renpho RP-BPM001

GUDID 00860002249605

JOICOM CORPORATION

Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

• Primary Device ID: 00860002249605
• NIH Device Record Key: 1ec85d6b-c7a5-488a-9331-b3be13dc9788
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: renpho
• Version Model Number: RP-BPM001
• Catalog Number: RP-BPM001
• 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	00860002249605 [Primary]
GS1	00860002249612 [Package]; Package: [40 Units]; Discontinued: 2020-02-16; Not in Commercial Distribution
GS1	10860002249602 [Package]; Package: [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: 3
• Public Version Date: 2020-02-17
• Device Publish Date: 2019-09-19

On-Brand Devices [renpho]

• 00860002249605: RP-BPM001
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• 10810140062137: Massage Gun