Christopher Toomes

FDA Filings

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

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



Registration Number3007710603
FEI Number3007710603
NameChristopher Toomes
Owner & OperatorXVIVO Perfusion AB
Contact Address3666 South Inca Street
Englewood CO 80110 US
Official Correspondent
  • Christopher - Toomes
  • 001-714-2139109-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address3666 South Inca Street
Englewood, CO 80110 US
Establishment TypeComplaint File Establishment per 21 CFR 820.198



FDA Filings

Device
Company
DeviceDate
Christopher Toomes [XVIVO PERFUSION LUND AB]
Silicone Tubing Set2019-11-25
Christopher Toomes [XVIVO Perfusion AB]
XVIVO PGM2019-11-23
Christopher Toomes [XVIVO Perfusion AB]
XVIVO Organ Chamber2019-11-23
Christopher Toomes [XVIVO Perfusion AB]
XVIVO Lung Cannula Set2019-11-23
Christopher Toomes [XVIVO Perfusion AB]
XVIVO Disposable Kit2019-11-23
Christopher Toomes [XVIVO Perfusion AB]
XPS2019-11-23
Christopher Toomes [XVIVO Perfusion AB]
XPS Disposable Lung Circuit2019-11-23
Christopher Toomes [XVIVO Perfusion AB]
STEEN Solution2019-11-23
Christopher Toomes [XVIVO Perfusion AB]
Perfadex Plus2019-11-23
Christopher Toomes [XVIVO Perfusion AB]
Silicone Tubing Set2013-05-07

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