34 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PATHROMTIN SL
FDA 510(k)
FDA Class 2
·Hematology
PATHROMTIN SL
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GFO·August 11, 2017
PATHROMTIN SL
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GFO·August 11, 2017
PATHROMTIN SL (RILIBAK)
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GFO·January 4, 2023
VENTRALIGHT
FDA UDI
Davol Inc.·00801741031717·Ventralight ST Mesh with Echo PS Positioning Sy...
Key Surgical Plastic Instruments
FDA UDI
KEY SURGICAL, INC.·00849771027867·Plastic Instruments, Sponge Forcep, 9.5-inch, p...
NA
FDA UDI
KEY SURGICAL, INC.·10849771050343·Plastic Instruments, Sponge Forcep, 9.5-inch, p...
Zuma
FDA UDI
Seaspine Orthopedics Corporation·10889981096878·Rasp, 38mm x 26mm x 10mm, 8 Deg
IN THE EAR HEARING AID
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
ADULT CIRCLE BREATH CIRCUIT W/INTERN GAS SAMP LINE
FDA 510(k)
FDA Class 1
·Anesthesiology
BAERVELDT SHUNT
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012
BAERVELDT SHUNT
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012
BAERVELDT SHUNT
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012
BAERVELDT SHUNT
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012
BAERVELDT SHUNT
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code KYF·September 5, 2012
BAERVELDT SHUNT
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code KYF·September 5, 2012
BAERVELDT SHUNT
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012
BAERVELDT SHUNT
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012
SYMBIQ DUAL CHANNEL
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·June 12, 2014
CAPSURE SP
FDA Adverse Event
Malfunction
·MPRI·Product code DTB·February 11, 2013