HENNIG ENTERPRISES EUROPE S.R.L.

FDA Registration(s)#

Registration, FEI, Name table
Registration	FEI	Name	Status	Initial importer	Expiration year	Address
9680787	3002826093	HENNIG ENTERPRISES EUROPE S.R.L.	1	N	2026-01-01	B-DUL POITIERS 14 IASI RO 700671

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration key	Listing key	Premarket submission	Device	Product code	Decision date
15218	1858533913	K910007	SPRINGFUSOR 10R	FRN	1993-11-02
15218	1877926379	K900336	V SET	FPA	1990-10-04
15218	2038710995	K890400	MODIFIED URINARY CATHETER INTRODUCER (UCI)	KOD	1989-09-12
15218	1501160604	K850758	AMNIGLOVE & AMNICOT	HGE	1985-04-15
15218	1501160604
15218	1577340188
15218	1703259416
15218	1791354396
15218	1858533913
15218	1877926379
15218	1958889910
15218	1961820990

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product code	Registration listing records	Latest decision
FRN	1	1993-11-02
FPA	1	1990-10-04
KOD	1	1989-09-12
HGE	1	1985-04-15

PMN#

V SET
2003-08-29
HENNIG ENTERPRISES EUROPE S.R.L.
GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES
2003-04-29
HENNIG ENTERPRISES EUROPE S.R.L.