FDA.reportPublic FDA data

TE ME NA SAS

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30053793873005379387TE ME NA SAS1N2020-04-2516, RUE DES ENTREPRENEURS Z.I des amandiers CARRIERES SUR SEINE Yvelines FR 78 420

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
544911811624337K991259TE ME NA EPIDURAL CATHETERBSO2001-02-21
544911035362639K990323TE ME NA POLYSTIM NERVE STIMILATORBXN2001-09-28
544911021364149K990100POLYMEDIC UPA NERVE STIMULATION NEEDLE; POLYMEDIC UPC NERVE STIMULATION NEEDLEGXZ2000-08-02
544911083881666K990020TE ME NA LOSS OF RESISTANCE SYRINGE, 10CCFMF1999-06-24
544911521786501K962329GLOBAL LOSS OF RESISTANCE SYRINGE GLOR 10FMF1996-09-12
544911564073695K940061POLYMEDIC SPINAL NEEDLE AND INTRODUCERBSP1995-12-21
544911220165809K854816EPIDURAL ANESTHESIA NEEDLESBSP1985-12-19
544912051853432K080603HYBRID NERVE LOCATION NEEDLE COATED AND UNCOATEDBSP2008-08-05
544911490399164K060186POLYPLEX STIMULATING CATHETER SYSTEMCAZ2006-07-18
544911073771138K002405SPINAL EPIDURAL NEEDLESBSP2001-06-01
544911837656168
544911932869649

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
BSP42008-08-05
FMF21999-06-24
CAZ12006-07-18
BXN12001-09-28
BSO12001-02-21
GXZ12000-08-02

PMN#