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iProven NCT-978

by Sevenground Trading B.V.

iProven NCT-978 is a Class II device made by Sevenground Trading B.V., listed in FDA GUDID since 2 Oct 2020 (UDI-DI 08719699635944), registry data as of 23 Oct 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08719699635944 UDI-DI Date2 Oct 2020ListedStatusListed 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  • Withdrawn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
iProven
Generic name
Infrared patient thermometer, skin
Model / reference
NCT-978
Primary DI / UDI-DI
08719699635944
FDA product code
FLL
GMDN term
Infrared patient thermometer, skin
Device class
Class II
Regulation number
880.2910
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FLL (Thermometer, Electronic, Clinical).

Other devices from Sevenground Trading B.V.

See all devices from Sevenground Trading B.V. →

Properties

  • Lot / batch number
Other properties (14, all answered No)