Nittobo Medical Co L T D Medical Development Center

FDA Filings

This page includes the latest FDA filings for Nittobo Medical Co L T D Medical Development Center. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number1000403749
FEI Number1000403749
NameNITTOBO MEDICAL CO., LTD. MEDICAL DEVELOPMENT CENTER
Owner & OperatorNittobo Medical Co., Ltd.
Contact Address1, Shiojima Fukuhara, Fukuyama
Koriyama JP-07 Hukusima 963-8061 JP
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1, Shiojima, Fukuhara Fukuyama
Koriyama Hukusima, 963-8061 JP
Establishment Type
  • Manufacture Medical Device
  • Manufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
NITTOBO MEDICAL CO., LTD. MEDICAL DEVELOPMENT CENTER [Nittobo Medical Co., Ltd.]
K-ASSAY Fibrinogen2008-01-31
NITTOBO MEDICAL CO., LTD. MEDICAL DEVELOPMENT CENTER [Nittobo Medical Co., Ltd.]
K-ASSAY Apo B2008-01-31
NITTOBO MEDICAL CO., LTD. MEDICAL DEVELOPMENT CENTER [Nittobo Medical Co., Ltd.]
N-ASSAY TIA Apo AI2008-01-31
NITTOBO MEDICAL CO., LTD. MEDICAL DEVELOPMENT CENTER [Nittobo Medical Co., Ltd.]
K-ASSAY Apo AI2008-01-31
NITTOBO MEDICAL CO., LTD. MEDICAL DEVELOPMENT CENTER [Nittobo Medical Co., Ltd.]
K-ASSAY CRP Calibrator2008-01-31

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