15 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STERILE RADIOLUCENT SKULL PINS
FDA 510(k)
FDA Class 2
·Neurology
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772814220·GENUMEDI PT SILVER L V
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X1222250·12mm H x 22mm W x 25mm L x 0 degrees XLIF
ELMED INCORPORATED
FDA UDI
ELMED INCORPORATED·00198506060830·Cushing Forceps, 1 x 2 Teeth, 10"
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L122225120·12mm H x 22mm W x 25mm L XLIF Trial 12 degree L...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X12222580·12mm H x 22mm W x 25mm L x 8 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L122250120·12mm H x 22mm W x 25mm L XLIF Trial 12 degree L...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X122225120·12mm H x 22mm W x 25mm L x 12 degrees XLIF
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970478·
ALCO-BREATH TUBE, CHECKPOINT BREATH ALCOHOL TEST
FDA 510(k)
FDA Class 1
·Clinical Toxicology
VECTOR MEDICAL, INC., VECTOR TARGETING SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ALLEGRETTO WAVE EYE-Q
FDA Adverse Event
Injury
·WAVELIGHT AG·Product code LZS·May 17, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 13, 2011
ACUITY CENTRAL STATION
FDA Adverse Event
Malfunction
·WELCH ALLYN PROTOCOL, INC.·Product code DSI·August 15, 2008
CP5 FLOW MODULE
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code DWA·July 18, 2024