Tokuyama Sekisui Co

FDA Filings

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

FDA Registration(s)
Registration Number3006850222
FEI Number3006850222
NameHiro Masumoto
Owner & OperatorTOKUYAMA SEKISUI CO.
Contact Address4560,Kaisei-cho
Shunan-City JP-35 Yamaguti 746-0006 JP
Official Correspondent
  • Masaaki Minamoto
  • 081-834-630951-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address50 W Big Beaver Rd, Ste 145
Troy, MI 48084 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
Hiro Masumoto [TOKUYAMA SEKISUI CO.]
BD Vacutainer Rapid Serum Tube (RST2010-08-16
Hiro Masumoto [TOKUYAMA SEKISUI CO.]
BD Vacutainer(R)2009-09-14

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