Mauricio Pineda

FDA Filings

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

FDA Registration(s)
Registration Number3009960884
FEI Number3009960884
NameMauricio Pineda
Owner & OperatorAsahi Kasei Medical Co., Ltd.
Contact Address1-1-2 Yurakucho
Chiyoda-ku JP-13 Tokyo 100-0006 JP
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1855 Elmdale Avenue
Glenview, IL 60026 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility

Registration Number8010002
FEI Number3002806407
NameMauricio Pineda
Owner & OperatorAsahi Kasei Medical Co., Ltd.
Contact Address1-1-2 Yurakucho
Chiyoda-ku JP-13 Tokyo 100-0006 JP
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1855 Elmdale Avenue
Glenview, IL 60026 US
Establishment Type
  • Manufacture Medical Device for Another Party (Contract Manufacturer)
  • Sterilize Medical Device for Another Party (Contract Sterilizer)

FDA Filings

Device
Company
DeviceDate
Mauricio Pineda [Asahi Kasei Medical Co., Ltd.]
Liposorber LA-15 system2018-06-21
Mauricio Pineda [Asahi Kasei Medical Co., Ltd.]
REXEED-S SERIES DIALYZERS2016-05-12
Mauricio Pineda [Asahi Kasei Medical Co., Ltd.]
REXEED-S SERIES DIALYZERS2016-05-12
Mauricio Pineda [Asahi Kasei Medical Co., Ltd.]
Liposorber LA-15 system2013-11-19
Mauricio Pineda [Asahi Kasei Medical Co., Ltd.]
Liposorber LA-15 system2013-01-30
Mauricio Pineda [Asahi Kasei Medical Co., Ltd.]
Plasmaflo OP-05W(A)2012-04-10
Mauricio Pineda [Asahi Kasei Medical Co., Ltd.]
Plasmaflo OP-05W(A)2012-04-10

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