RENPHO

GUDID 00810140061300

Smart Foot and Calf Massager

Joicom Corporation

Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager

• Primary Device ID: 00810140061300
• NIH Device Record Key: b6df4eb1-2153-4ca4-bf3f-8714eb2e69dd
• Commercial Distribution Discontinuation: 2034-05-14
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RENPHO
• Version Model Number: R-D001RS
• 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	00810140061300 [Primary]

FDA Product Code

• ISA: Massager, Therapeutic, Electric

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: 2024-05-23
• Device Publish Date: 2024-05-15

On-Brand Devices [RENPHO ]

• 00860002249605: RP-BPM001
• 10810140061864: Massage Gun
• 00810140061300: Smart Foot and Calf Massager