Transcutaneous Electrical Nerve Stimulator For Pain Relief

GUDID 06924607702980

Shenzhen Kentro Medical Electronics Co.,Ltd

Analgesic transcutaneous electrical nerve stimulation system

• Primary Device ID: 06924607702980
• NIH Device Record Key: c1b67a3d-d267-4a36-957c-0880716ec80e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Transcutaneous Electrical Nerve Stimulator For Pain Relief
• Version Model Number: KTR-2412
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06924607702980 [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: 2024-12-25
• Device Publish Date: 2024-12-17

On-Brand Devices [Transcutaneous Electrical Nerve Stimulator For Pain Relief ]

• 06924607702942: KTR-2302
• 06924607702980: KTR-2412
• 06924607702973: KTR-2411
• 06924607702966: KTR-2402
• 06924607702959: KTR-2401