Sirtex Wilmington L L C

FDA Filings

This page includes the latest FDA filings for Sirtex Wilmington L L C. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3005579300
FEI Number3005579300
NameSirtex Wilmington LLC
Owner & OperatorSirtex Medical Pty Ltd
Contact AddressShop 6 207 Pacific Highway
St Leonards AU-NSW New South Wales 2065 AU
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address16 Upton Drive Unit 2-4
Wilmington, MA 01887 US
Establishment Type
  • Manufacture Medical Device
  • Repack or Relabel Medical Device

FDA Filings

Device
Company
DeviceDate
Sirtex Wilmington LLC [Sirtex Medical Pty Ltd]
SIR-Spheres2007-10-23
Sirtex Wilmington LLC [Sirtex Medical Pty Ltd]
SIR-Spheres microspheres2007-10-23
Sirtex Wilmington LLC [Sirtex Medical Pty Ltd]
SIR-Spheres Delivery Box2003-12-19
Sirtex Wilmington LLC [Sirtex Medical Pty Ltd]
SIR-Spheres V-Vial Holder2003-12-19
Sirtex Wilmington LLC [Sirtex Medical Pty Ltd]
Syringe Shield2003-12-19
Sirtex Wilmington LLC [Sirtex Medical Pty Ltd]
V-Vial2003-12-19
Sirtex Wilmington LLC [Sirtex Medical Pty Ltd]
SIR-Spheres V-Vial2003-12-19
Sirtex Wilmington LLC [Sirtex Medical Pty Ltd]
SIR-Spheres Delivery Set2003-12-19
Sirtex Wilmington LLC [Sirtex Medical Pty Ltd]
SIR-Spheres Accessories Pack2003-12-19

Related Finance Registrations
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
202001082956Hong Kong,Hong Kong -> New York/Newark Area, Newark, New JerseyV VIAL HOLDER36 CTN
202001016624Hong Kong,Hong Kong -> New York/Newark Area, Newark, New JerseyV VIAL HOLDER36 CTN
2019073122252Singapore,Singapore -> New York/Newark Area, Newark, New JerseySIRTEX V VIAL HOLDER (BASE PLUG CAP) HS CODE: 3923.90001 PKG
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