11 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NAVISCAN PEMFLEX SOLO II HIGH RESOLUTION PET SCANNER
FDA 510(k)
FDA Class 2
·Radiology
PRECISION XTRA BLOOD GLUCOSE TEST STRIP WITH TRUEMEASURE TECHNOLOGY
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ARKIT HBA1C
FDA 510(k)
FDA Class 2
·Hematology
ROD, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019
ILIAC SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code MNH·October 16, 2019
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE·Product code KDJ·May 2, 2013
DURA DURATION A/P TIB SM 11
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·September 15, 2014
TRIDENT 10" X3 INSERT 32MM ID
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS MAHWAH·Product code LPH·April 19, 2011
POLARIS SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code NKB·January 8, 2020
3M TEGADERM ALGINATE AG SILVER DRESSING
FDA Adverse Event
Injury
·3M HEALTH CARE·Product code FRO·June 21, 2016
POLARIS TRANSLATION SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019