16 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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PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
CD HORIZON® Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994168948·ROD 7893075 6.35MM X 75MM PEEK ROD
Chromophare F300
FDA UDI
Berchtold Holding GmbH·07613327297768·Berchtold Examination Light ? Mobile
Sirca
FDA UDI
Berchtold Holding GmbH·07613327616569·
Osteo3 ZP Putty
FDA 510(k)
FDA Class 2
·Orthopedic
ARAGON SURGICAL RF SYSTEM TELEO INSTRUMENT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CAIMAN DISP. INSTR. NON ARTICUL. D:5/360MM
FDA Adverse Event
Malfunction
·AESCULAP AP & CO. KG·Product code GEI·March 27, 2015
CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO KG·Product code GEI·April 6, 2015
NOVATION
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JDI·January 31, 2023
CAIMAN DISP.INSR.ARTICULAT.D:12 / 240MM
FDA Adverse Event
Malfunction
·AESCULAP AG& CO. KG·Product code GEI·April 15, 2015
CAIMAN DISP INSTR ARTICULAT D:12/240MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO KG·Product code GEI·April 16, 2014
ARTICULEZE M HEAD 36MM +1.5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·June 24, 2014
TERUMO PERFUSION SYSTEM 8000
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code JOR·November 2, 2010
RESTORE ULTRA
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·January 2, 2013
CAIMAN DISP. INSTR. ARTICULAT. D.: 12/440MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code GEI·July 28, 2014
MOBILE EXAMINATION LIGHT F 300, LED, DIMMABLE, W/EXTRA WEIGHT, 100-120 V(AC) W/S
FDA Adverse Event
Injury
·BERCHTOLD GMBH & CO. KG·Product code KZF·September 11, 2019