Iberhospitex S A

FDA Filings

This page includes the latest FDA filings for Iberhospitex 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 Number3009191041
FEI Number3009191041
NameMatt Clausen
Owner & OperatorIberhospitex S.A.
Contact AddressAvda. Catalunya, 4
Llica de Vall ES-B Barcelona 08185 ES
Official Correspondent
  • Matt Clausen
  • 34-93-8436034-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1200 Townline Road
Mundelein, IL 60060 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
IBERHOSPITEX, S.A.
DRENOVAC1989-02-23
IBERHOSPITEX, S.A.
SANIFIX1988-12-13
IBERHOSPITEX, S.A.
OPER-FILM-ADHESIVE MEMBRANE1988-08-31

Related Finance Registrations
NCAGE Code0955BIBERHOSPITEX SA
CAGE Code0955BIBERHOSPITEX SA
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
201908213367Barcelona ,Spain -> Miami, FloridaMEDICAL SUPPLIES120 PKG
201908203820Barcelona ,Spain -> Miami, FloridaMEDICAL SUPPLIES120 PKG
201908193423Barcelona ,Spain -> Miami, FloridaMEDICAL SUPPLIES120 PKG
2019041223953Valencia,Spain -> Miami, FloridaINTO 2 PKGS DRESSINGS51 PKG
2018022613417Barcelona ,Spain -> Miami, FloridaFREIGHT PREPAID ON 25 PALLETS MEDICAL SUPPLIES720 PCS
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.