23 results · 21ms · Sources: EU EUDAMED, US FDA

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ALARA CRYSTALVIEW COMPUTED RADIOGRAPHY SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

Baltic Denture System BD Load

FDA UDI
Merz Dental GmbH·D7091032210·Baltic Denture System BDLoad Mn6 PLSEbim6DFm A2...

Audit MicroControls Control FD Assayed Chemistry, Level 2

FDA UDI
AALTO SCIENTIFIC·B085K0312100·

SOAR Retractor System

FDA UDI
SPINEOLOGY INC.·M7403032210·22MM X 100MM Tube

Battalion

FDA UDI
ALPHATEC SPINE, INC.·00840967187587·Battalion, LLIF Trial, 10°, 22 mm Wide, 10 mm X...

NIDO Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07315K0122100·T-Handle, Head Persuader

SYNTRA DIALYZER, MODEL SYNTRA 120, 160

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

MODIFICATION TO ACCU-CHEK INFORM METER

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

SCP PANEL CENTRIFUGE JMS

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DWA·November 5, 2013

S4 IMPLANTS

FDA Adverse Event
Malfunction ·AESCULAP AG & CO. KG·Product code KWP·August 29, 2008

SCP PANEL CENTRIFUGE JMS

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DWA·March 14, 2014

SCP CONTROL PANEL

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·January 5, 2012

CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP

FDA Adverse Event
Malfunction ·LIVANOVA DEUTSCHLAND·Product code DWA·January 19, 2018

CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP

FDA Adverse Event
Malfunction ·LIVANOVA DEUTSCHLAND GMBH·Product code DWA·January 5, 2022

STOCKERT JMS CENTRIFUGAL PUMP SYSTEM

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·January 5, 2012

DELTA VALVE, SMALL, PERFORMANCE LEVEL 1.5

FDA Adverse Event
Injury ·MEDTRONIC NEUROSURGERY·Product code JXG·March 29, 2013

PUNCH, STD 2.75MM, 15 DEG UP CURVED

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code MDM·March 29, 2011

COOK TPN CATHETER SET

FDA Adverse Event
Malfunction ·COOK INC·Product code DQY·April 18, 2008

STOCKERT CENTRIFUGAL PUMP (SCP) SYSTEM

FDA Adverse Event
Injury ·SORIN GROUP DEUTSCHLAND·Product code DWA·May 7, 2010

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code NEK·March 21, 2011