POLE ELECTRODE PEN TYPE

GUDID 14897076721143

TENS PLUS INDUSTRIAL COMPANY

External manual massager, clinical

• Primary Device ID: 14897076721143
• NIH Device Record Key: 0fa7618c-3887-4f48-bb0e-d4cd9833131f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: POLE ELECTRODE PEN TYPE
• Version Model Number: PtP.Probe
• 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	14897076721143 [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: 2022-11-22
• Device Publish Date: 2022-11-14

On-Brand Devices [POLE ELECTRODE PEN TYPE]

• 14897076721143: PtP.Probe
• 14897076721136: A4.Pen