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iProvèn BBB-112 Grey

by Sevenground Trading B.V.

iProvèn BBB-112 Grey is a Class II device made by Sevenground Trading B.V., listed in FDA GUDID since 30 Jun 2023 (UDI-DI 08719699636644), 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 Number08719699636644 UDI-DI Date30 Jun 2023ListedStatusListed 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  • Withdrawn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
iProvèn
Generic name
Insect bite/sting hyperthermia device
Model / reference
BBB-112 Grey
Primary DI / UDI-DI
08719699636644
FDA product code
IRT
GMDN term
Insect bite/sting hyperthermia device
Device class
Class II
Regulation number
890.5740
GUDID distribution status
In Commercial Distribution

Related devices

Category: Insect bite/sting hyperthermia device

Similar devices

Other devices filed under FDA product code IRT (Pad, Heating, Powered).

Other devices from Sevenground Trading B.V.

See all devices from Sevenground Trading B.V. →

Properties

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