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 Number: 3004756837
• FEI Number: 3004756837
• Name: PENTAFERTE ITALIA S.R.L.
• Owner & Operator: PENTAFERTE ITALIA s.r.l.
• Contact Address: Viale Piane Nocella, 23 ; CAMPLI IT-TE Teramo 64012 IT
• US Agent:
  • Luca Giustini
  • PQE US
  • 267 7958865
  • l.giustini@pqegroup.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: Viale Piane Nocella, 23 ; CAMPLI Teramo, 64012 IT
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
PMN K214080 PENTAFERTE ITALIA S.R.L.	Pentaflush	2022-07-20
PMN K161141 | PNR PENTAFERTE ITALIA S.R.L.	NUTRIFIT	2018-07-30
PMN K002381 | FMF PENTAFERTE ITALIA S.R.L.	CRN CRONO SYRINGE RESERVOIR	2018-05-15
PMN K161141 PENTAFERTE ITALIA S.R.L.	ENFit Enteral Pump Syringes PENTA ENFit, ENFit Enteral Pump Syringes NUTRIFIT	2017-03-22