12 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
STRYKER S2 DRILL
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
CENTERVUE DIGITAL RETINOGRAPHY SYSTEM
FDA 510(k)
FDA Class 2
·Ophthalmic
DR SYSTEMS PACS, RELEASE 6.1
FDA 510(k)
FDA Class 2
·Radiology
PLEURX LOCKABLE DRAINAGE LINE SET
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code DWM·April 2, 2026
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 4, 2014
OT PING 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 28, 2011
PLEURX
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code DWM·September 26, 2025
LOGIC CR FEMORAL POR, LEFT, SZ 4
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·March 27, 2024
TRULIANT TIB FIT TRAY CEM SZ 4F / 3T
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·January 13, 2025
THREE PEG PATELLA 32MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·January 13, 2025
PLEURX
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code DWM·June 2, 2025