14 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Shoreline ACS Interbody System; Shoreline RT Interbody System
FDA 510(k)
FDA Class 2
·Orthopedic
n.a.
FDA UDI
Karl Storz GmbH & Co. KG·04048551082171·Elevator, tip 15°, 1 mm, 18 cm
Reprocessed Oscillating/Sagittal Saw Blade, Thick, 25 x 5.5 x 0.56mm
FDA UDI
SURETEK MEDICAL·B390KM334141·
Brasseler USA
FDA UDI
Provision·00810041064998·
Brasseler USA
FDA UDI
Provision·B504OMKM334140·
SMALL BONE BLADES
FDA UDI
Peter Brasseler Holdings, LLC·00887919094319·KM33-414
NA
FDA UDI
STERILMED, INC.·10888551017145·SAW BLADE MICRO OSCILLATING 12 TEETH/CM STRYKER...
ELMED
FDA UDI
ELMED INCORPORATED·00842180168480·Whelan Femoral Neck Elevator, Overall Length: ...
REPROCESSED CLOSURE SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ACL TOP MODEL, TOP
FDA 510(k)
FDA Class 2
·Hematology
INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code OYC·November 6, 2014
ACCESS
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MALTA·Product code FPA·September 2, 2011
MBT REVISION CEM TIB TRAY S1.5
FDA Adverse Event
Injury
·1818910 DEPUY ORTHOPAEDICS, INC.·Product code NJL·July 18, 2013
MEDFUSION 4000 WIRELESS SYRINGE INFUSION PUMP
FDA Adverse Event
Malfunction
·ST PAUL·Product code FRN·June 8, 2022