Asahi Kasei Medical Mt Corp Okatomi Plant

FDA Filings

This page includes the latest FDA filings for Asahi Kasei Medical Mt Corp Okatomi Plant. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3007340888
FEI Number3007340888
NameAsahi Kasei Medical MT Corp. Okatomi Plant
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 Address5-4960 NAKAGAWARA-MACHI
NOBEOKA-SHI Miyazaki, 882-0031 JP
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
Asahi Kasei Medical MT Corp. Okatomi Plant [Asahi Kasei Medical Co., Ltd.]
REXEED-S SERIES DIALYZERS2016-05-12

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