11 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SUNMED'S GREENLINE FIBER OPTIC LARYNGOSCOPE
FDA 510(k)
FDA Class 1
·Anesthesiology
LEVEL ONE CMF
FDA UDI
KLS-Martin L.P.·00888118093721·MESH, SPECIALTY, BEALS, LADDER, 2.0 MM SCREW, T...
PLAYTEX ULTIMATES UNSCENTED/SCENTED TAMPONS
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
THE ANSWER HEARING AID
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.35 WIRE, 12, STERILE
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code GCP·August 11, 2021
MAXIMO II CRT-D
FDA Adverse Event
Injury
·IPG MFG SWITZERLAND·Product code NIK·February 11, 2013
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·January 10, 2011
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·UNKNOWN·Product code IOR·July 24, 2014
HF-RESECTION ELECTRODE
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code GCP·March 8, 2023
HF-RESECTION ELECTRODE
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code GCP·March 8, 2023
UNKNOWN
FDA Adverse Event
Injury
·OLYMPUS WINTER & IBE GMBH·Product code KNS·October 21, 2022