16 results
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34ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STAYHEALTHY HEALTH KIOSK, STAYHEALTHY HEALTHCENTER KIOSK
FDA 510(k)
FDA Class 2
·Cardiovascular
QUANTA SYSTEM DUOLITE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
STERI-SPOUTS; BAG-SPOUT, VIAL-SPOUT, TRANSFER MIXER; RAPIDFLOW, VIALFLOW, TRANSFLOW
FDA 510(k)
FDA Class 2
·General Hospital
MUST LT 25MM LONG - PEDICLE SCREW Ø5X45 FENESTRATED
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKB·December 7, 2021
ROD, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019
5.5 TI CANNULATED TRANSLATION SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019
M2A 38MMX54MM CUP
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·May 22, 2013
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·September 26, 2014
PYXIS ANESTHESIA SYSTEM (PAS)
FDA Adverse Event
Malfunction
·CAREFUSION·Product code BRY·June 9, 2011
ILIAC SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code MNH·October 16, 2019
POLARIS SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code NKB·January 8, 2020
ARTIS Q ZEEGO
FDA Adverse Event
Malfunction
·SIEMENS HEALTHINEERS AG·Product code OWB·December 10, 2024
CANNULATED TRANSLATION SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code NKB·December 3, 2020
POLARIS CURVED ROD, UNKNOWN
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code MNH·November 27, 2019
POLARIS TRANSLATION SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019
POLARIS CURVED ROD, UNKNOWN
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code MNH·November 27, 2019