29 results
·
21ms
·
Sources: EU EUDAMED, US FDA
AEMED STIMPAD ACU-TENS TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR, MODEL 021999
FDA 510(k)
FDA Class 2
·Neurology
PMMA disc
FDA UDI
Dentsply International Inc.·D00180711200·
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704292626·
CONMED
FDA UDI
Conmed Corporation·10845854000281·OSCILLATOR BLADE, 19.5 X 95 X 0.9 MM (.035")
NA
FDA UDI
STERILMED, INC.·10888551020336·SAW BLADE OSCILLATING LARGE BONE
GLUCOPRO INFUSION SET, MODEL GPISXXXXXXXX SERIES
FDA 510(k)
FDA Class 2
·General Hospital
ENVOY PATIENT MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·April 22, 2013
FREESTYLE NAVIGATOR
FDA Adverse Event
Malfunction
·Product code LFR·April 27, 2011
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·July 10, 2008
ONYX
FDA Adverse Event
Injury
·COVIDIEN (IRVINE)·Product code MFE·May 1, 2015
ARCOS STS DIST STEM 24X250MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·December 8, 2025
BATTERY POWERDRIVER P2
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code GEY·September 28, 2021
PLATE 4 HOLE WITH GAP 2.0MM
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code JEY·September 28, 2021
BATTERY POWERDRIVER P2
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code GEY·September 28, 2021
BATTERY POWERDRIVER P2
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code GEY·September 28, 2021
BATTERY POWERDRIVER P2
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code GEY·September 28, 2021
BATTERY POWERDRIVER P2
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code GEY·September 28, 2021
LACTO SCR 1.5X5MM 1.5 SYS 2PK
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code JEY·September 28, 2021
BATTERY POWERDRIVER P2
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code GEY·September 28, 2021