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hetaida H8830US

by Hetaida Technology Co., Ltd 2 variants

hetaida H8830US is a Class II device made by Hetaida Technology Co., Ltd, listed in FDA GUDID since 16 Oct 2026 (UDI-DI 06970289035953), registry data as of 2 Nov 2026.

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

Source GUDID, synced 2 Nov 2026.

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06970289035953 UDI-DI Date16 Oct 2026ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
hetaida
Generic name
Infrared patient thermometer, skin
Model / reference
H8830US
Primary DI / UDI-DI
06970289035953
FDA product code
SDV
GMDN term
Infrared patient thermometer, skin
Device class
Class II
Regulation number
880.2910
GUDID distribution status
In Commercial Distribution

Other devices from Hetaida Technology Co., Ltd.

See all devices from Hetaida Technology Co., Ltd. →

Properties

  • Premarket exempt
  • Lot / batch number
Other properties (13, all answered No)