41 results
·
20ms
·
Sources: EU EUDAMED, US FDA
CRYOCARE CARDIAC SURGICAL SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Endo Carry-on Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964153044·Endo Carry-on Procedure Kit contains Basin, VIA...
LoFric®
FDA UDI
Wellspect AB·07333387035741·Single Use Urinary Catheter LoFric Nelaton 8" 1...
LoFric®
FDA UDI
Wellspect AB·07392532135231·Single Use Urinary Catheter LoFric Nelaton 8" 1...
MEGA PLUS SPINE SYSTEM
FDA UDI
BK MEDITECH CO.,LTD.·08809763502293·Final Wrench (BT20)(Short)
CitreLock 4.0mm Reamer
FDA UDI
Acuitive Technologies, Inc.·00810027270023·
MedaSonics
FDA UDI
Coopersurgical, Inc.·00888937002515·Versatone D8 Doppler 220V AC
General Instruments
FDA UDI
ALPHATEC SPINE, INC.·00811801033544·Modular Compressor Distractor - Offset R
HRH-127 HEAD ARRAY COIL
FDA 510(k)
FDA Class 2
·Radiology
SLEEVED FILTER
FDA 510(k)
FDA Class 2
·Anesthesiology
PENTAX
FDA Adverse Event
Injury
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·March 5, 2021
PENTAX
FDA Adverse Event
Injury
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·March 5, 2021
SM104 MSERIES W5TH
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FPO·February 14, 2012
NA
FDA UDI
Orthosoft Inc·00889024305397·
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·November 28, 2020
M2A-MAGNUM MOD HD
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·May 15, 2017
SORBAFIX ENHANCED
FDA Adverse Event
Injury
·DAVOL INC., SUB. C.R. BARD, INC.·Product code GDW·March 12, 2013
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·March 8, 2011
PERV. VENT. LINEAR BIPOLAR
FDA Adverse Event
Injury
·TELECTRONICS PACING SYSTEMS·Product code DTB·March 10, 2008
M2A-MAGNUM 42-50MM TPR INSRT-6
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·May 15, 2017