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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