Cup.Long.xD

GUDID 14897076722850

TENS PLUS INDUSTRIAL COMPANY

Cupping therapy device Cupping therapy device Cupping therapy device Cupping therapy device Cupping therapy device Cupping therapy device Cupping therapy device Cupping therapy device Cupping therapy device Cupping therapy device Cupping therapy device Cupping therapy device Cupping therapy device Cupping therapy device Cupping therapy device Cupping therapy device Cupping therapy device

• Primary Device ID: 14897076722850
• NIH Device Record Key: c65b2770-9002-4290-a57c-6be0aa66b1b0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cup.Long.xD
• Version Model Number: DY0444
• 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	14897076722850 [Primary]

FDA Product Code

• KNM: Device, Pressure Applying

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: 2023-03-23
• Device Publish Date: 2023-03-15

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