HY-Impact Massager

GUDID 00674986031107

TV Direct LLC

Hand-held electric massager

• Primary Device ID: 00674986031107
• NIH Device Record Key: caf1f616-c110-4ce8-9887-6778c371dc3b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HY-Impact Massager
• Version Model Number: Regular
• Company DUNS: 078829674
• Company Name: TV Direct LLC
• 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: true
• 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	00674986031107 [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: 2023-05-22
• Device Publish Date: 2023-05-12

Devices Manufactured by TV Direct LLC

• 00674986037826 - HY IMIPACT CUPPING MASSAGER: 2024-01-23
• 00674986031107 - HY-Impact Massager: 2023-05-22
• 00674986031107 - HY-Impact Massager: 2023-05-22
• 00674986032548 - HY-Impact Nano: 2023-05-22