33 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PROTECH DENT
FDA 510(k)
FDA Unclassified
·Unknown
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772813827·GENUMEDI PRO SILVER SIZE II
ArgenZ Anterior 95x16 #6
FDA UDI
ARGEN CORPORATION, THE·D818121272·Dental porcelain/ceramic restoration kit
Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780180319·Integra® Jarit® Fell Needle Holder, 7", Carb-Bi...
Bonopty Penetration Set
FDA UDI
Apriomed AB·07350031352726·Manually operated, sterile, single use coaxial ...
Bonopty Penetration Set
FDA UDI
Apriomed AB·07350031350302·Manually operated, sterile, single use coaxial ...
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970430·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973691·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973073·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970447·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973905·
MASS OXYGEN DISTRIBUTION SYSTEM (MODS) MODEL 10C-0061-3
FDA 510(k)
FDA Class 2
·Anesthesiology
SIB CATHETER, MODEL 61-7005
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
COOK-SWARTZ DOPPLER PROBE
FDA Adverse Event
Injury
·COOK VANDERGRIFT INC·Product code ITX·April 4, 2022
COOK-SWARTZ DOPPLER PROBE
FDA Adverse Event
Injury
·COOK VANDERGRIFT INC·Product code ITX·February 22, 2022
COOK-SWARTZ DOPPLER PROBE
FDA Adverse Event
Injury
·COOK VANDERGRIFT INC·Product code ITX·February 2, 2022
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013
SERISCAFFOLD SURGICAL SCAFFOLD (OUS)
FDA Adverse Event
Injury
·ALLERGAN·Product code OXF·September 22, 2014
AC POWER MODULE
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code MKJ·May 4, 2011
COOK-SWARTZ DOPPLER PROBE
FDA Adverse Event
Injury
·COOK VANDERGRIFT INC·Product code ITX·November 23, 2022