Xvivo Perfusion Lund Ab

FDA Filings

This page includes the latest FDA filings for Xvivo Perfusion Lund Ab. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

Xvivo Perfusion Lund Ab holds import registrations or U.S. agent authorizations in conjunction with the following organizations:

FDA Registration(s)
Registration Number3013516772
FEI Number3013516772
NameChristopher Toomes
Owner & OperatorXVIVO PERFUSION LUND AB
Contact Address3666 South Inca Street
Englewood CO 80110 US
Official Correspondent
  • Christopher Toomes
  • 01-303-3033959-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address3666 South Inca Street
Englewood, CO 80110 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Christopher Toomes [XVIVO PERFUSION LUND AB]
Silicone Tubing Set2019-11-25

Related Finance Registrations

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