Skip to content

EmeTerm YF-ZTY-E2

by WAT Medical Technology Inc. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06971760281487 UDI-DIDate23 Apr 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
EmeTerm
Generic Name
Anti-nausea transcutaneous electrical nerve stimulation wristband
Model / Reference
YF-ZTY-E2
Primary DI / UDI-DI
06971760281487
510(k) Number
FDA Product Code
GZJ
GMDN Term
Anti-nausea transcutaneous electrical nerve stimulation wristband
Device Class
Class II
Regulation Number
882.5890
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K220503)

Other devices from WAT Medical Technology Inc.

See all devices from WAT Medical Technology Inc. →

Properties

  • Over-the-Counter
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No