Alexandre Delemazure

FDA Filings

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

FDA Registration(s)
Registration Number3011274144
FEI Number3011274144
NameAlexandre DELEMAZURE
Owner & OperatorWESTLAKE PLASTICS EUROPE
Contact Address2 rue de Maestricht
TOURCOING FR-59 Nord 59200 FR
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address490 LENNI RD
Lenni, PA 19052 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
Alexandre DELEMAZURE [WESTLAKE PLASTICS EUROPE]
MADISON2020-01-29
Alexandre DELEMAZURE [WESTLAKE PLASTICS EUROPE]
SURGICAL INSTRUMENTS2018-06-18

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