29 results
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25ms
·
Sources: EU EUDAMED, US FDA
VTS1000
FDA 510(k)
FDA Class 1
·General Hospital
SEMIAL 10°
FDA UDI
SIGNUS Medizintechnik GmbH·04047844000908·The KIMBA®, KIMBA® mini, MOBIS® and NOVAL™ impl...
TeleSenseRCM
FDA UDI
SCOTTCARE CORPORATION, THE·00856298006022·The TeleSense device is intended for diagnostic...
Sklar®
FDA UDI
SKLAR CORPORATION·10649111003707·E-Z LOCK INSTR STRINGER 5X18"
CENTRIFUGAL PUMP
FDA 510(k)
FDA Class 2
·Cardiovascular
ERGO IMAGING SYSTEM
FDA 510(k)
FDA Class 1
·Radiology
Widex
FDA UDI
Widex A/S·05706069726923·Widex EVOKE E-PA (Sporty red S-110 ) RC coil
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·April 29, 2025
PRECISION SPECTRA
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·August 16, 2019
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·May 1, 2013
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 10, 2011
SOLETRA
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·August 7, 2008
3.0MM TI W/ MAXBRAID SUTURE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code HWC·October 4, 2012
3.0MM TI W/ MAXBRAID SUTURE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code HWC·October 4, 2012
THROMBUSTER II
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code MMY·March 17, 2014
3.0MM TI W/ MAXBRAID SUTURE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code HWC·October 4, 2012
THROMBUSTER II
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code DXE·October 23, 2012
THROMBUSTER II
FDA Adverse Event
Malfunction
·KANEKA CORP.·Product code DXE·December 21, 2012
THROMBUSTER II
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code DXE·January 16, 2019
EUFLEXXA
FDA Adverse Event
Injury
·BIO-TECHNOLOGY GENERAL (ISRAEL) LTD.·Product code MOZ·February 23, 2015