Neomedic I N T

FDA Filings

This page includes the latest FDA filings for Neomedic I N T. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3004838863
FEI Number3004838863
NameNEOMEDIC INTERNATIONAL
Owner & OperatorNEOMEDIC INTERNATIONAL
Contact AddressC/ MAESTRAT 41-43 1
TERRASSA ES-B Barcelona 08225 ES
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressMAESTRAT 41-43
TERRASA Barcelona, 08225 ES
Establishment TypeExport Device to the United States But Perform No Other Operation on Device



FDA Filings

Device
Company
DeviceDate
NEOMEDIC INTERNATIONAL
SURELIFT PROLAPSE SYSTEM2011-07-07

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