22 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
HCG CONTROL
FDA 510(k)
FDA Class 1
·Clinical Chemistry
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772813865·GENUMEDI PRO SILVER SIZE VI
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471150584·K-WIRE - DOUBLE TROCAR 1.0mm DIA x 150mm
Instrument Case
FDA UDI
KATENA PRODUCTS, INC.·00841668111017·SILICONE MAT FOR INSTRUMENT CADDY
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471122925·K-WIRE - DOUBLE TROCAR 1.2mm DIA x 150mm
Life Instruments
FDA UDI
Life Instrument Corporation·M9307921206W0·Washer for Cup Positioner
Life Instruments
FDA UDI
Life Instrument Corporation·M9307921206B320·32mm Ball
Life Instruments
FDA UDI
Life Instrument Corporation·M930792120600·Cup Positioner
Life Instruments
FDA UDI
Life Instrument Corporation·M9307921206B0·Cup Positioner 28mm Ball
IMMULITE 2000 3GALLERGY SPECIFIC IGE
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED·Product code DHB·May 22, 2018
IMMULITE 2000 SPECIFIC ALLERGENS
FDA 510(k)
FDA Class 2
·Immunology
DETECT
FDA 510(k)
FDA Unclassified
·Unknown
Life Instruments
FDA UDI
Life Instrument Corporation·M9307921206010·Custom Cup Positioner
IMMULITE 2000 3GALLERGY SPECIFIC IGE
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED·Product code DHB·May 22, 2018
PRECISION
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 9, 2010
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·January 17, 2013
MOTORIZED 3-WHEELED VEHICLE FOR OUTSIDE TRANSPORT
FDA Adverse Event
C.T.M. SHANGHAI·Product code INI·July 9, 2014
90 DEGREE SCREWDRIVER T-HANDLE
FDA Adverse Event
Malfunction
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWE·September 24, 2020
IOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX SYSTEM
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code QJR·May 5, 2021
BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX SYSTEM
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code QJR·May 5, 2021