Pentaferte Italia S R L

FDA Filings

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

FDA Registration(s)
Registration Number3004756837
FEI Number3004756837
NamePENTAFERTE ITALIA S.R.L.
Owner & OperatorPENTAFERTE ITALIA s.r.l.
Contact AddressViale Piane Nocella, 23
CAMPLI IT-TE Teramo 64012 IT
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressViale Piane Nocella, 23
CAMPLI Teramo, 64012 IT
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
PENTAFERTE ITALIA S.R.L.
Pentaflush2022-07-20
PENTAFERTE ITALIA S.R.L.
NUTRIFIT2018-07-30
PENTAFERTE ITALIA S.R.L.
CRN CRONO SYRINGE RESERVOIR2018-05-15
PENTAFERTE ITALIA S.R.L.
ENFit Enteral Pump Syringes PENTA ENFit, ENFit Enteral Pump Syringes NUTRIFIT2017-03-22

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