35 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LIPOKIT
FDA Adverse Event
Malfunction
·OSYRIS MEDICAL·Product code GEX·April 6, 2010
OSIRIS
FDA 510(k)
FDA Class 2
·Radiology
v900L Vision System
FDA UDI
SYRIS SCIENTIFIC LLC·00867009000406·Polarized Illumination System with magnificatio...
v300H Vision System
FDA UDI
SYRIS SCIENTIFIC LLC·00867009000413·Polarized Illumination System with magnificatio...
Syris VTS1000 Battery
FDA UDI
DermLite LLC·00850017651388·Syris VTS1000 Battery
Syris v900L Charging Base
FDA UDI
DermLite LLC·00850017651609·Syris v900L Charging Base
Syris VTS1000 Power Supply
FDA UDI
DermLite LLC·00850017651371·Syris VTS1000 Power Supply
Syris v900L Control Module
FDA UDI
DermLite LLC·00850017651357·Syris v900L Control Module
Syris v900L Visualization System
FDA UDI
DermLite LLC·00850017651289·Illuminated headlamp with adjustable polarizati...
Syris v900L Illuminator Module
FDA UDI
DermLite LLC·00850017651340·Syris v900L Illuminator Module
Syris v900L Charger & Battery
FDA UDI
DermLite LLC·00850017651333·Syris v900L Charger & Battery
GLACIER
FDA UDI
SDI LIMITED·DO3670141421·
ICE
FDA UDI
SDI LIMITED·DO3684000191·
WAVE
FDA UDI
SDI LIMITED·DO3675141421·
O Series OR Pad - Gel Mattress Family
FDA UDI
SIZEWISE RENTALS, L.L.C.·00845699004416·
NP "O" Series OR Pad - Foam Mattress Family
FDA UDI
SIZEWISE RENTALS, L.L.C.·00845699002900·
ALLEGRETTO WAVE EYE-Q
FDA Adverse Event
Injury
·WAVELIGHT GMBH·Product code LZS·September 29, 2014
PORTEX HYPODERMIC NEEDLE-PRO EDGE SAFETY WITH SYRI
FDA Adverse Event
Malfunction
·NULL·Product code MEG·September 11, 2022
BARDIA® FOLEY CATHETER SILICONE COATED
FDA Adverse Event
Malfunction
·C.R. BARD INC. (COVINGTON) -1018233·Product code KOD·August 15, 2024
MENTOR MEMORYGEL BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·October 6, 2024