40 results · 26ms · Sources: EU EUDAMED, 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