Bionen S A S

FDA Filings

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

FDA Registration(s)
Registration Number3008617703
FEI Number3008617703
NameBIONEN S.A.S
Owner & OperatorBionen s.a.s
Contact AddressVia P. Petrocchi, 42/1
Florence IT-FI Firenze 50127 IT
Official Correspondent
  • Monia Nencioni
  • 039-055-4265945-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressVia P. Petrocchi, 42/1
Florence Firenze, 50127 IT
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
BIONEN S.A.S
Disposable Monopolar/Subdermal Needle Electrode2010-11-02
BIONEN S.A.S
Disposable Monopolar Needle Electrode2010-11-02
BIONEN S.A.S
Disposable Concentric Needle Electrode2010-11-02
BIONEN S.A.S
Disposable Monopolar/Subdermal Needle Electrode2010-11-02
BIONEN S.A.S
Disposable Monopolar Needle Electrode2010-11-02
BIONEN S.A.S
Disposable Concentric Needle Electrode2010-11-02
BIONEN S.A.S.
DISPOSABLE AND REUSABLE CONCENTRIC NEEDLES / DISPOSABLE AND REUSABLE MONOPOLAR NEEDLE2010-10-07

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