8 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Multi-Lancet Device 2, ReliOn Premier Lancing Device
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
J & J INSTRUMENTS
FDA UDI
J & J INSTRUMENTS INC·00817524025507·OPERATING SCI 5.5"" B/B CVD
TriVerse Femoral Trial PS Insert
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215097813·
FLASH PTA BALLON DILATATION CATHETER-5MM X 19MM X 135CM
FDA 510(k)
FDA Class 2
·Cardiovascular
AERONEB PROFESSIONAL NEBULIZER SYSTEM, MODEL#AG-AP6000
FDA 510(k)
FDA Class 2
·Anesthesiology
RESTORE
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·November 3, 2014
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE·Product code KDJ·August 24, 2011
M2A-MAGNUM 42-50MM TPR INSRT-3
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·July 11, 2013