19 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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THERA-MIST HUMIDIFIER
FDA 510(k)
FDA Class 2
·Anesthesiology
TW DRILL 1.1X50MM 15MMSTP W/NT
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HBE·November 9, 2021
Snowden-Pencer
FDA UDI
STERIS CORPORATION·10885403156212·Snowden-Pencer DIAMOND-LINE DISSECTOR BIOPSY FO...
SurgiCount
FDA UDI
STRYKER CORPORATION·07613327622751·+ Sponge Counting Software
Triton
FDA UDI
STRYKER CORPORATION·07613327622768·AI Software
Triton
FDA UDI
STRYKER CORPORATION·07613327622775·QBL Software
SurgiCount
FDA UDI
STRYKER CORPORATION·07613327622799·+ QBL Software
N/A
FDA UDI
STRYKER CORPORATION·07613327622782·SC+ AI Software
TANDEM VISUAL HCG IMMUNOENZYMETRIC
FDA 510(k)
FDA Class 2
·Clinical Chemistry
RIONET HEARING AID HB-73
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
LONG NAIL KIT R2.0, TI, LEFT GAMMA3 ?11X400MM X 13
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·December 4, 2012
SNOWDEN PENCER
FDA Adverse Event
Other
·CAREFUSION 2200, INC.·Product code GEI·March 29, 2024
OXFORD PARTIAL KNEE SYSTEM RIGHT MEDIAL TIBIAL TRAY
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·June 21, 2017
ITOTAL G2
FDA Adverse Event
Injury
·CONFORMIS·Product code JWH·June 17, 2014
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·November 3, 2010
SYSTEM 5 RECIP/STERNUM SAW
FDA Adverse Event
Injury
·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·December 21, 2012
OXFORD PARTIAL KNEE SYSTEM TWIN PEG FEMORAL
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·June 21, 2017
1.5MM SYSTEM TWIST DRILL WITH J NOTCH 1.1 X 50MM, 15MM STOP
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HBE·November 24, 2020
3.0MM PRCSN MTCH HD, 13CM
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-KALAMAZOO·Product code HBE·June 13, 2019