Hennig Enterprises Europe S R L

FDA Filings

This page includes the latest FDA filings for Hennig Enterprises Europe 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 Number9680787
FEI Number3002826093
NameRobert Dean
Owner & OperatorHENNIG ENTERPRISES EUROPE S.R.L.
Contact AddressB-DUL POITIER 14 --
IASI RO-NOTA 700671 RO
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1083 Delaware Ave
Buffalo, NY 14209 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
Robert Dean [HENNIG ENTERPRISES EUROPE S.R.L.]
Springfusor and FCT2008-02-03
Robert Dean [HENNIG ENTERPRISES EUROPE S.R.L.]
V-Set2008-02-03
Robert Dean [HENNIG ENTERPRISES EUROPE S.R.L.]
O'Neil Sterile Field Urinary Catheter2008-02-03
Robert Dean [HENNIG ENTERPRISES EUROPE S.R.L.]
Amnicot2008-02-03
HENNIG ENTERPRISES EUROPE S.R.L.
V SET2003-08-29
HENNIG ENTERPRISES EUROPE S.R.L.
GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES2003-04-29

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