26 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER KIT AND SET
FDA 510(k)
FDA Class 2
·Anesthesiology
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772813834·GENUMEDI PRO SILVER SIZE III
CHANG CHOPPER
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896072534·CHANG CHOPPER COMBINATION RIGHT ANGLED MICROSCO...
CHANG COMBINATION CHOPPER/MICROSOPIC FINGER
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896013063·CHANG COMBINATION CHOPPER/MICROSOPIC FINGER RIG...
TAPERLOC®
FDA UDI
Biomet Orthopedics, LLC·00880304430693·
ELI 250 ELECTROCARDIOGRAPH
FDA 510(k)
FDA Class 2
·Cardiovascular
HA MALLORY/HEAD POROUS FEMORAL STEM & HA MALLORY/HEAD POROUS LATERALIZED FEMORAL STEM
FDA 510(k)
FDA Class 2
·Orthopedic
M-H HA/PC 11X160MM T1
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·December 16, 2015
EASYSPINE SCREW, UNKOWN SIZE OR TYPE
FDA Adverse Event
Injury
·LDR MEDICAL·Product code NKB·August 17, 2020
M-H SOLID SHELL HA/PC DIA54MM LN24
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·March 1, 2016
MALLORY-HEAD SHORT FEMORAL STEM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code MEH·July 28, 2017
PRONTO SPOT CHECK PULSE CO-OXIMETER
FDA Adverse Event
Malfunction
·MASIMO - 40 PARKER·Product code DQA·July 9, 2018
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013
VS3: NBP, SP02, TEMP
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code MHX·May 5, 2011
3M LOBAN 2 ANTIMICROBIAL DRAPE
FDA Adverse Event
Other
·3M HEALTH CARE·Product code KKX·August 13, 2008
MALLORY-HEAD ACETABULAR SHELL 54MM POUROUS + HAP COATED
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code MEH·August 11, 2016
MLRY-HD XR LAT POR FMRL 8MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·August 24, 2020
EASY SPINE SCREW, UNKNOWN
FDA Adverse Event
Injury
·LDR MEDICAL·Product code NKB·March 24, 2020
EASY SPINE ROD, UNKNOWN
FDA Adverse Event
Injury
·LDR MEDICAL·Product code NKB·March 24, 2020
EASY SPINE SCREW, UNKNOWN
FDA Adverse Event
Injury
·LDR MEDICAL·Product code NKB·March 24, 2020