RENPHO

GUDID 00810140062093

Joicom Corporation

Bioelectrical body composition analyser

• Primary Device ID: 00810140062093
• NIH Device Record Key: 13110953-694b-4b0c-872a-d31cd1a515cd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RENPHO
• Version Model Number: ES-CS20M
• Company DUNS: 033774836
• Company Name: Joicom Corporation
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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	00810140062093 [Primary]

FDA Product Code

• PUH: Analyzer, Body Composition, Exempt

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: 2024-10-21
• Device Publish Date: 2024-10-11

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• 00810140062093: ES-CS20M
• 10810140062113: Massage Gun
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• 10810140062120: Massage Gun