RENPHO Eye Massager

GUDID 10810140060393

Joicom Corporation

Hand-held electric massager

• Primary Device ID: 10810140060393
• NIH Device Record Key: 14d88a83-786b-453e-81d7-1a87f5a42331
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RENPHO Eye Massager
• Version Model Number: RF-EM001
• 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	00810140060396 [Primary]
GS1	10810140060393 [Package]; Contains: 00810140060396; Package: case [16 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: 2023-08-15
• Device Publish Date: 2023-08-07

On-Brand Devices [RENPHO Eye Massager]

• 10810140061185: R-G010V
• 10810140060492: R-G006
• 10810140060485: R-G006
• 10810140060478: R-G006
• 10810140060461: R-G004
• 10810140060447: RF-EM001R
• 10810140060430: RF-EM001R
• 10810140060393: RF-EM001
• 10810140060386: RF-EM001
• 10810140060379: RF-EM001