EmeTerm

GUDID 06971760280015

TENS device-EmeTerm generates the electric pulses with highly specific waveforms, frequency and amplitude to stimulate the median nerve. The accurate pulse signals provide relief through electrical stimulation of the nerves in the patient’s wrist.

WAT Medical Technology Inc.

Anti-nausea transcutaneous electrical nerve stimulation wristband Anti-nausea transcutaneous electrical nerve stimulation wristband Anti-nausea transcutaneous electrical nerve stimulation wristband Anti-nausea transcutaneous electrical nerve stimulation wristband Anti-nausea transcutaneous electrical nerve stimulation wristband Anti-nausea transcutaneous electrical nerve stimulation wristband Anti-nausea transcutaneous electrical nerve stimulation wristband Anti-nausea transcutaneous electrical nerve stimulation wristband Anti-nausea transcutaneous electrical nerve stimulation wristband Anti-nausea transcutaneous electrical nerve stimulation wristband Anti-nausea transcutaneous electrical nerve stimulation wristband Anti-nausea transcutaneous electrical nerve stimulation wristband Anti-nausea transcutaneous electrical nerve stimulation wristband Anti-nausea transcutaneous electrical nerve stimulation wristband Anti-nausea transcutaneous electrical nerve stimulation wristband Anti-nausea transcutaneous electrical nerve stimulation wristband Anti-nausea transcutaneous electrical nerve stimulation wristband

• Primary Device ID: 06971760280015
• NIH Device Record Key: 1b677fb1-9d62-49f8-a543-5bc7ce094239
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EmeTerm
• Version Model Number: YF-ZTY-E1
• Company DUNS: 544509582
• Company Name: WAT Medical Technology Inc.
• 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: false
• 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	06971760280015 [Primary]
GS1	16971760280012 [Package]; Package: box [60 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K172478

FDA Product Code

• GZJ: Stimulator, Nerve, Transcutaneous, For Pain Relief

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: 2021-12-08
• Device Publish Date: 2021-11-30

On-Brand Devices [EmeTerm]

• 06971760280015: TENS device-EmeTerm generates the electric pulses with highly specific waveforms, frequency and
• 16971760281088: TENS device-EmeTerm generates the electric pulses with highly specific waveforms, frequency and
• 16971760281033: TENS device-EmeTerm generates the electric pulses with highly specific waveforms, frequency and
• 16971760281019: TENS device-EmeTerm generates the electric pulses with highly specific waveforms, frequency and
• 16971760281309: TENS device-EmeTerm generates the electric pulses with highly specific waveforms, frequency and