16 results · 23ms · Sources: EU EUDAMED, US FDA

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SOL PORTABLE DIODE LASER UNIT (WITH WIRELESS FOOT CONTROL)

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

APPLIANCE, FIXATION, SPINAL INTERLAMINAL

FDA Adverse Event
Injury ·SYNTHES USA·Product code KWP·March 31, 2016

VTS1000

FDA 510(k)
FDA Class 1 ·General Hospital

MPS (OR MPS-T)

FDA 510(k)
FDA Class 2 ·Neurology

AP409 -PRIMARY INFUSION SET WITH VENTED/NON-VENTED DRIP CHAMBER

FDA Adverse Event
Malfunction ·EITAN MEDICAL LTD.·Product code FPA·December 18, 2025

AP205 - INFUSION SET WITH NON-VENTED SPIKE, 1.2UM FILTER AND NEEDLE Y-SITE

FDA Adverse Event
Malfunction ·EITAN MEDICAL LTD.·Product code FPA·June 5, 2024

AP210 - MICROBORE WITH NON-VENTED SPIKE AND 1.2UM FILTER

FDA Adverse Event
Malfunction ·EITAN MEDICAL LTD.·Product code FPA·June 6, 2024

AP210 - MICROBORE WITH NON-VENTED SPIKE AND 1.2UM FILTER

FDA Adverse Event
Malfunction ·EITAN MEDICAL LTD.·Product code FPA·June 17, 2024

AP403 - MICROBORE INFUSION SET WITH VENTED/NON-VENTED SPIKE

FDA Adverse Event
Malfunction ·EITAN MEDICAL LTD.·Product code FPA·March 31, 2026

1.6MM X 14MM FULL THREADED SCREW, LOCKING

FDA Adverse Event
Malfunction ·OSTEOMED, LLC·Product code HWC·March 31, 2021

1.6MM, 3 X 8 HOLES, "Y" PLATE

FDA Adverse Event
Malfunction ·OSTEOMED, LLC·Product code HRS·March 31, 2021

1.6MM X 16MM FULL THREADED SCREW, LOCKING

FDA Adverse Event
Malfunction ·OSTEOMED, LLC·Product code HWC·March 31, 2021

AP407 - INFUSION SET WITH VENTED/NON-VENTED DRIP CHAMBER AND NEEDLELESS Y-SITE

FDA Adverse Event
Malfunction ·EITAN MEDICAL LTD.·Product code FPA·March 4, 2026

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 4, 2014

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 27, 2011