Skip to content

Auvon TU1080

by Ansion Technology (GuangDong) Co. Ltd. 5 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850085485038 UDI-DI Date26 Jun 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Auvon
Generic Name
Analgesic transcutaneous electrical nerve stimulation system
Model / Reference
TU1080
Primary DI / UDI-DI
00850085485038
FDA Product Code
NUH, NGX
GMDN Term
Analgesic transcutaneous electrical nerve stimulation system
Device Class
Class II
Regulation Number
882.5890, 890.5850
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Other devices from Ansion Technology (GuangDong) Co. Ltd.

See all devices from Ansion Technology (GuangDong) Co. Ltd. →

Properties

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

Other properties (11)

  • 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
  • Expiration Date: No