42 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HEMOSTASIS MANAGEMENT SYSTEM PLUS (HMS PLUS ), MODEL 305 XX
FDA 510(k)
FDA Class 2
·Hematology
Preat
FDA UDI
Preat Corporation·00842092108383·Preci-Clix 1271
Transducer Cover
FDA UDI
CIVCO MEDICAL INSTRUMENTS CO., INC.·10841436102923·Sterile (14 x 147cm) telescopically-folded cover
Mercodia Glucagon ELISA
FDA UDI
Mercodia AB·07350108630122·Mercodia Glucagon ELISA is an assay intended to...
Mercodia Glucagon ELISA
FDA UDI
Mercodia AB·07350108630115·Mercodia Glucagon ELISA is an assay intended to...
POWDER-FREE LATEX EXAMINATION GLOVE, BLUE COLORED
FDA 510(k)
FDA Class 1
·General Hospital
SAMARCO SPIDER PLATES
FDA 510(k)
FDA Class 2
·Orthopedic
SPECTRA WAVEWRITER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 23, 2023
AS VEGA PS TIBIAL PLATEAU CEMENTED T3
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code JWH·April 4, 2018
VASO VIEW HEMOPRO
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR LLC·Product code GEI·April 8, 2019
ATLAS PLUS VR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 9, 2013
TPS HANDPIECE CORD
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-KALAMAZOO·Product code EIA·September 19, 2014
CAPSURE SP NOVUS
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·May 24, 2011
VASOVIEW HEMOPRO 2
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR LLC·Product code GEI·April 13, 2019
HEMOPRO 2 ADAPTOR
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR LLC·Product code GEI·February 21, 2020
AS COLUMBUS REV F FEMUR CEMENTED F5L
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code JWH·April 3, 2018
AS VEGA PS TIBIAL PLATEAU CEMENTED T3+
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code JWH·April 3, 2018
AS VEGA PS TIBIAL PLATEAU CEMENTED T2
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code JWH·April 3, 2018
AS COLUMBUS REV F TIB.OFFSET CEMENT.T5
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code JWH·April 3, 2018
AS VEGA PS FEMORAL COMP.CEMENTED F5N R
FDA Adverse Event
Malfunction
·AESCULAP IMPLANT SYSTEMS·Product code JWH·March 23, 2018