40 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SpeediCath Flex Coude Pro
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Portex
FDA UDI
ICU MEDICAL, INC.·00351688038237·
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613017958·K-Wire, Double Ended, Trocar Point, Diameter 0....
Hayden Medical
FDA UDI
Hayden Medical, Inc.·00840319741658·Rhoton buttoned probe, curved 90°, 7-1/2" (19cm)
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306822797·Yankauer Suction Tube, 35cm
QUIKCLOT INTEVENTIONAL, MODEL P/N 182
FDA 510(k)
FDA Unclassified
·Unknown
FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR , MODEL KN-550
FDA 510(k)
FDA Class 2
·Cardiovascular
EARLYVUE VS30 VITAL SIGNS MONITOR
FDA Adverse Event
Malfunction
·PHILIPS NORTH AMERICA LLC·Product code DSJ·September 15, 2021
EARLYVUE VS30 VITAL SIGNS MONITOR
FDA Adverse Event
Malfunction
·PHILIPS NORTH AMERICA LLC·Product code DSJ·March 1, 2022
EARLYVUE VS30 VITAL SIGNS MONITOR
FDA Adverse Event
Malfunction
·PHILIPS NORTH AMERICA LLC·Product code DSJ·August 1, 2022
BIOLOX DELTA CER LNR 36MM E
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LZO·February 5, 2026
RINGLOC-X E1 H/W 56/36MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·April 27, 2026
BIOLOX DELTA CER LNR 40MM G
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·April 27, 2026
BIPHASIC LIFEPAK 500 AUTOMATED EXTERNAL DEFIBIRLLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·October 3, 2008
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 4, 2011
ACCU-CHEK ® AVIVA PLUS TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·June 26, 2013
REVOLUTION (ASSEMBLED INTO CUSTOMISED PERFUSION TUBING)
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA·Product code KFM·December 11, 2025
EARLYVUE VS30 VITALS MONITOR
FDA Adverse Event
Malfunction
·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code DSJ·June 14, 2021
EARLYVUE VS30 VITALS MONITOR
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MHX·July 29, 2021
AVAN E1 INSERT 28 S 52
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·March 6, 2025