Transcutaneous Electrical Nerve Stimulator For Pain Relief

GUDID 06924607702942

Shenzhen Kentro Medical Electronics Co.,Ltd

Analgesic transcutaneous electrical nerve stimulation system Analgesic transcutaneous electrical nerve stimulation system Analgesic transcutaneous electrical nerve stimulation system Analgesic transcutaneous electrical nerve stimulation system Analgesic transcutaneous electrical nerve stimulation system Analgesic transcutaneous electrical nerve stimulation system Analgesic transcutaneous electrical nerve stimulation system Analgesic transcutaneous electrical nerve stimulation system Analgesic transcutaneous electrical nerve stimulation system Analgesic transcutaneous electrical nerve stimulation system Analgesic transcutaneous electrical nerve stimulation system Analgesic transcutaneous electrical nerve stimulation system Analgesic transcutaneous electrical nerve stimulation system Analgesic transcutaneous electrical nerve stimulation system Analgesic transcutaneous electrical nerve stimulation system Analgesic transcutaneous electrical nerve stimulation system Analgesic transcutaneous electrical nerve stimulation system Analgesic transcutaneous electrical nerve stimulation system

• Primary Device ID: 06924607702942
• NIH Device Record Key: 84ca8ad5-ac1e-43b9-bf47-5936cfe647fb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Transcutaneous Electrical Nerve Stimulator For Pain Relief
• Version Model Number: KTR-2302
• Company DUNS: 544395368
• Company Name: Shenzhen Kentro Medical Electronics Co.,Ltd
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• 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	06924607702942 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K232517

FDA Product Code

• NUH: Stimulator, Nerve, Transcutaneous, Over-The-Counter

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: 2024-01-24
• Device Publish Date: 2024-01-16

Devices Manufactured by Shenzhen Kentro Medical Electronics Co.,Ltd

• 06924607702942 - Transcutaneous Electrical Nerve Stimulator For Pain Relief: 2024-01-24
• 06924607702942 - Transcutaneous Electrical Nerve Stimulator For Pain Relief: 2024-01-24
• 06924607702683 - Transcutaneous Electrical Nerve Stimulator: 2023-12-11
• 06924607702706 - Transcutaneous Electrical Nerve Stimulator: 2023-12-11
• 06924607702713 - Transcutaneous Electrical Nerve Stimulator: 2023-12-11
• 06924607702720 - Transcutaneous Electrical Nerve Stimulator: 2023-12-11
• 06924607702737 - Transcutaneous Electrical Nerve Stimulator: 2023-12-11
• 06924607702744 - Transcutaneous Electrical Nerve Stimulator: 2023-12-11
• 06924607702751 - Transcutaneous Electrical Nerve Stimulator: 2023-12-11