JUMBO ROLLER

GUDID 14897076721075

TENS PLUS INDUSTRIAL COMPANY

Static magnetic massager

• Primary Device ID: 14897076721075
• NIH Device Record Key: c2805d06-2ba5-423d-bdbe-f52d6fc183c1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: JUMBO ROLLER
• Version Model Number: Drum.Jumbo
• Company DUNS: 663211978
• Company Name: TENS PLUS INDUSTRIAL COMPANY
• 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	14897076721075 [Primary]

FDA Product Code

• LYG: Massager, Therapeutic, Manual

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: 2022-11-22
• Device Publish Date: 2022-11-14

Devices Manufactured by TENS PLUS INDUSTRIAL COMPANY

• 14897076721457 - Lion.Warm.XL: 2023-06-13
• 14897076721655 - Multi.D.1.5: 2023-06-13
• 14897076721815 - Moxa.Bx.BamS: 2023-06-13
• 14897076721822 - Moxa.Bx.BamL: 2023-06-13
• 14897076721853 - Pistol: 2023-06-13
• 14897076721860 - Pistol.Long: 2023-06-13
• 14897076721877 - Ins.MP.S: 2023-06-13
• 14897076721884 - Ins.MP.M: 2023-06-13