38 results
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26ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Riptide Aspiration System
FDA 510(k)
FDA Class 2
·Cardiovascular
OsteoMed
FDA UDI
OSTEOMED LLC·00845694027342·2.4mm X 48mm Cannulated Headless Screw
OsteoMed
FDA UDI
OSTEOMED LLC·00845694069168·Cannulated 2.4 x 48mm Headless Screw Sterile Qty 2
PULSIOFLEX
FDA 510(k)
FDA Class 2
·Cardiovascular
VARIANT II TURBO HbA1c Kit - 2.0
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·August 6, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·August 6, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·August 6, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·October 17, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·November 9, 2018
ROSA ONE
FDA Adverse Event
Injury
·MEDTECH SA·Product code HAW·January 11, 2019
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code NAY·January 21, 2019
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·December 21, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·November 15, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·November 15, 2018
OPTIPAC 60 REFOB BONE CMT R-3
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code LOD·May 11, 2026
CAMERA HANDLE, W/RIDGE ALUMINUM
FDA Adverse Event
Malfunction
·STRYKER-COMMUNICATIONS·Product code FSY·June 17, 2013
TOTALCARE BARIATRIC
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·June 17, 2011
COBAS 6000 C501MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code CEM·September 19, 2008
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·November 15, 2018