Oldelft Benelux B V

FDA Filings

This page includes the latest FDA filings for Oldelft Benelux B V. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3006476569
FEI Number3006476569
NameOLDELFT BENELUX BV
Owner & OperatorOldelft Benelux BV
Contact AddressWiltonstraat 41
Veenendaal NL-UT Utrecht 3905 KW NL
Official Correspondent
  • Luc Wijnhoven
  • 31-6-43795437-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressWiltonstraat 41
Veenendaal Utrecht, 3905 KW NL
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
OLDELFT BENELUX BV
Single Shot Stitch Frame2019-10-09
OLDELFT BENELUX BV
Single Shot Long-Length Imaging Stand2019-10-09
OLDELFT BENELUX BV
One Shot Stitch Frame2019-10-09
OLDELFT BENELUX BV
One Shot Long-Length Imaging Stand2019-10-09
OLDELFT BENELUX BV
LLS-12019-10-09
OLDELFT BENELUX BV
LLS-1 Stitch Frame2019-10-09

Related Finance Registrations
NCAGE CodeHE714OLDELFT BENELUX B.V.
NCAGE CodeH1F27OLDELFT BENELUX B.V.
CAGE CodeH1F27OLDELFT BENELUX B.V.
CAGE CodeHE714OLDELFT BENELUX B.V.
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2020033032701Anvers,Belgium -> Miami, FloridaMEDICAL EQUIOMENT3 PKG
2020011154436Anvers,Belgium -> Miami, FloridaMEDICAL EQUIPMENT1 PKG
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