RENPHO Eye Massager

GUDID 10810140060409

Joicom Corporation

Hand-held electric massager

• Primary Device ID: 10810140060409
• NIH Device Record Key: bc85a820-9350-41ee-a47a-7f9f58357c0d
• 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	00810140060402 [Primary]
GS1	10810140060409 [Package]; Contains: 00810140060402; 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]

• 10810140060423: RF-EM001R
• 10810140060416: RF-EM001R
• 10810140060409: RF-EM001
• 10810140060362: RF-EM001
• 10810140060355: RF-EM001