Runlite S A

FDA Filings

This page includes the latest FDA filings for Runlite S A. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number8020160
FEI Number6347
NameRUNLITE S.A.
Owner & OperatorRUNLITE SA
Contact Address9 AVENUE DE LA COOPERATION, MICHEROUX
SOUMAGNE BE-NOTA 4630 BE
Official Correspondent
  • CHRISTIAN - HICK
  • 32-4377-3026-x
US Agent
Importing Logistics Registration
ImporterALLARD USA INC
Address300 Forge Way, Suite 3
Rockaway, NJ 07866 UNITED STATES
Importer TypeAgent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address9 AVENUE DE LA COOPERATION MICHEROUX
SOUMAGNE Liege, 4630 BE
Establishment TypeRepack or Relabel Medical Device



FDA Filings

Device
Company
DeviceDate
RUNLITE S.A. [RUNLITE SA]
X-LIFE1989-07-20
RUNLITE S.A. [RUNLITE SA]
X-LITE1989-07-20
RUNLITE S.A. [RUNLITE SA]
X-LITE1989-07-20
RUNLITE S.A. [RUNLITE SA]
X-LITE1989-07-20
RUNLITE S.A. [RUNLITE SA]
X-LITE1987-04-03

Related Finance Registrations
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2019103117033Anvers,Belgium -> Los Angeles, CaliforniaVARAFORM HS CODE 5903 90103 PKG
2019102922219Anvers,Belgium -> Los Angeles, CaliforniaVARAFORM HS CODE 5903 90103 PKG
2019102822085Anvers,Belgium -> Los Angeles, CaliforniaVARAFORM HS CODE 5903 90103 PKG
201803261212Anvers,Belgium -> Los Angeles, CaliforniaVARAFORM HS CODE 5903 90103 PKG
2018022725671Anvers,Belgium -> Long Beach, CaliforniaVARAFORM HS CODE 5903 90103 PKG

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