17 results
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40ms
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Sources: EU EUDAMED, US FDA
NEURAXIS, INC
FDA registration
NEURAXIS, INC·4 products·🇺🇸 United States
NSS IB-STIM
FDA UDI
Neuraxis, Inc.·B960NSS203·The IB-STIM (DEN180057) is a percutaneous elect...
NSS NeuroStim
FDA UDI
Neuraxis, Inc.·B960NSS201·The NSS Neurostim ((510K-140530) is a percutane...
RED
FDA UDI
Neuraxis, Inc.·B960RED201·The Rectal Expulsion Device (RED) is a catheter...
RED Prep-Kit
FDA UDI
Neuraxis, Inc.·B960RED202·The Rectal Expulsion Device Prep-kit (RED Prep-...
NSS-2 Bridge
FDA UDI
Neuraxis, Inc.·B960NSS200·The NSS-2 BRIDGE is a percutaneous nerve field ...
IB-STIM
FDA Adverse Event
Injury
·NEURAXIS, INC.·Product code QHH·June 30, 2023
IB-STIM
FDA Adverse Event
Injury
·NEURAXIS, INC.·Product code QHH·June 30, 2023
IB-STIM
FDA Adverse Event
Injury
·NEURAXIS INC·Product code QHH·June 24, 2025
BARD® DIGNISHIELD® STOOL MANAGEMENT SYSTEM
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNT·October 11, 2023
EPIDURAL ANESTHESIA KIT
FDA Adverse Event
Injury
·B. BRAUN MEDICAL INC.·Product code OGE·March 21, 2023
UNKNOWN EXTERNAL DRAINAGE AND MONITORING SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC MEXICO·Product code GWM·April 30, 2024
BARD® DIGNISHIELD® STOOL MANAGEMENT SYSTEM
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNT·December 19, 2023
PM050-N HYHSURGPN,7.5",EXP KT,-,OQ,5
FDA Adverse Event
Malfunction
·AVANOS MEDICAL INC.·Product code BSO·July 21, 2022
Epidural tray. PERIFIX 17 Ga. x 3-1/2 in. (90 mm) Tuohy, PERIFIX FX 19 Ga. Springwound Closed Tip Catheter, 5 mL Glass Luer Lock LOR Tray (Kit)-A collection of devices intended for the administration of an analgesic or anesthetic agent to the epidural space for the management of pain. Product Code: 332079
FDA Recall
Open, Classified
·B. Braun Medical, Inc.·Product code OGE·January 22, 2024
Epidural tray. PERIFIX 17 Ga. x 3-1/2 in. (90 mm) Tuohy, 5 mL Glass Luer Lock LOR Tray (Kit) A collection of devices intended for the administration of an analgesic or anesthetic agent to the epidural space for the management of pain. It includes the pharmaceutical anesthetic agent and a needle, with additional devices utilized for the procedure (e.g., syringe, dressings), and may include a catheter (i.e., may be intended for single- or continuous-administration). It is not intended for intrathecal anesthesia. Product Code: 332248
FDA Recall
Open, Classified
·B. Braun Medical, Inc.·Product code OGE·January 22, 2024
CERENOVUS EMBOGUARD
FDA Adverse Event
Malfunction
·CERENOVUS, INC. / NEURAVI LIMITED·Product code QJP·December 22, 2022