Identity
- Trade Name
- EmeTerm FDA UDI
- Generic Name
- Anti-nausea transcutaneous electrical nerve stimulation wristband FDA UDI
- Device Name
- 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. FDA UDI
- Model / Reference
- YF-ZTY-E1 FDA UDI
- Description
- 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. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06971760280787 FDA UDI
- 510(k) Number
- K172478 FDA UDI
- FDA Product Code
- GZJ FDA UDI
- GMDN Term
- Anti-nausea transcutaneous electrical nerve stimulation wristband FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.5890 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
Yes
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Anti-nausea transcutaneous electrical nerve stimulation wristband
EmeTerm by Wat Medical Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Anti-nausea transcutaneous electrical nerve stimulation wristband.
- Reliefband® Premier Charcoal — ReliefBand Technologies · Class II
- Reliefband® Premier Plus — ReliefBand Technologies · Class II
- Reliefband® Flex — ReliefBand Technologies · Class II
- Reliefband® Conductivity Gel — ReliefBand Technologies · Class II
- Reliefband® Custom USB Charging Cable — ReliefBand Technologies · Class II
- Reletex — ReliefBand Technologies · Class II
- Reliefband® 50 Hours — ReliefBand Technologies · Class II
- Reliefband® Sport - Black — ReliefBand Technologies · Class II
Cleared under the same submission
K172478 also covers:
- EmeTerm — Wat Medical Technology, Inc.
- EmeTerm — Wat Medical Technology, Inc.
- EmeTerm — Wat Medical Technology, Inc.
- EmeTerm — Wat Medical Technology, Inc.
- EmeTerm — Wat Medical Technology, Inc.
- EmeTerm — Wat Medical Technology, Inc.
- EmeTerm — Wat Medical Technology, Inc.
- EmeTerm — Wat Medical Technology, Inc.
- EmeTerm — Wat Medical Technology, Inc.
- EmeTerm — Wat Medical Technology, Inc.
- EmeTerm — Wat Medical Technology, Inc.
- EmeTerm — Wat Medical Technology, Inc.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Wat Medical Technology, Inc.
Sources (1)
- FDA UDI acfeab29-5e5a-42af-8b8e-ff3960320e84 34 fields · synced May 31, 2026