RENPHO Massage Gun

GUDID 10810140060171

Joicom Corporation

Hand-held electric massager

• Primary Device ID: 10810140060171
• NIH Device Record Key: 04926935-25af-407b-8349-77cf099c91dd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RENPHO Massage Gun
• Version Model Number: R-C001S
• 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	00810140060174 [Primary]
GS1	10810140060171 [Package]; Contains: 00810140060174; Package: case [6 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 Massage Gun]

• 10810140060348: R-C007
• 10810140060331: R-C001
• 10810140060324: RP-GM171-N1
• 10810140060317: RP-GM171-N1
• 10810140060300: R-C003H
• 10810140060294: R-C004
• 10810140060287: R-C004
• 10810140060218: RF-GM168
• 10810140060201: RF-GM168
• 10810140060195: R-C005
• 10810140060188: R-C003
• 10810140060171: R-C001S
• 10810140060164: R-C001