RENPHO

GUDID 00810140062000

Foot Massager

Joicom Corporation

Hand-held electric massager

• Primary Device ID: 00810140062000
• NIH Device Record Key: e8d77a9f-8426-42ff-b87d-409c9ca45d2a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RENPHO
• Version Model Number: R-WMF04
• 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	00810140062000 [Primary]
GS1	10810140062007 [Package]; Package: Case [4 Units]; In Commercial Distribution

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: 2024-08-26
• Device Publish Date: 2024-08-16

On-Brand Devices [RENPHO ]

• 00860002249605: RP-BPM001
• 10810140061864: Massage Gun
• 00810140061300: Smart Foot and Calf Massager
• 00810140061966: Foot Mssager
• 00810140062000: Foot Massager
• 00810140062093: ES-CS20M
• 10810140062113: Massage Gun
• 10810140062106: Massage Gun
• 10810140062120: Massage Gun
• 10810140062137: Massage Gun