Skip to content

TempBuddy ZTP-800

by Shenzhen Yuezhongxing Technology Co., Ltd. 2 variants

Listed FDA GUDID listing, not in commercial distribution

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 Number06971209168010 UDI-DI Date20 Nov 2025ListedStatusListed GUDID: not 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  • Withdrawn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
TempBuddy
Generic Name
Infrared patient thermometer, skin
Model / Reference
ZTP-800
Primary DI / UDI-DI
06971209168010
FDA Product Code
SDV
GMDN Term
Infrared patient thermometer, skin
Device Class
Class II
Regulation Number
880.2910
GUDID distribution status
Not in Commercial Distribution

Other devices from Shenzhen Yuezhongxing Technology Co., Ltd.

See all devices from Shenzhen Yuezhongxing Technology Co., Ltd. →

Properties

  • Convenience Kit
  • Lot / Batch Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No