Norgesplaster A S

FDA Filings

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

FDA Registration(s)
Registration Number3003810724
FEI Number3003810724
NameNORGESPLASTER AS
Owner & OperatorNORGESPLASTER A/S
Contact AddressGRANLIVEIEN 21
VENNESLA 4700 NO-10 Vest-Agder 85 NO
US Agent
Importing Logistics Registration
ImporterSmart Practice
Address3400 East Mcdowell Road Phoenix, AZ 85008
Phoenix, AZ 85008 UNITED STATES
Importer Typeinitial importer
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressGRANLIVEIEN 21
VENNESLA 4700 Vest-Agder, 85 NO
Establishment TypeManufacture Medical Device




Related Finance Registrations
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2020052835086Ystad,Sweden -> New York/Newark Area, Newark, New JerseySCANTAPE HS CODE: 560313001 PCS
2019082627141Stadersand,Federal Republic of Germany -> Los Angeles, CaliforniaMEDICAL TAPE1 PKG
2019032617594Stadersand,Federal Republic of Germany -> Los Angeles, CaliforniaSCANPORE TAPE1 PKG
2018121412882Stadersand,Federal Republic of Germany -> Los Angeles, CaliforniaSCANPOR TAPE3 PKG
2018031540565Anvers,Belgium -> New York/Newark Area, Newark, New JerseySCANTAPE5 PKG
201801039988Gothenburg,Sweden -> New York/Newark Area, Newark, New JerseyMEDICAL TAPE3 PKG

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.