32 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ASAHI ASTATO 30 PERIPHERAL GUIDE WIRE, MODELS - PAGH18M071, PAGH18M371
FDA 510(k)
FDA Class 2
·Cardiovascular
PASCO MIC AND MIC/ID PANELS
FDA 510(k)
FDA Class 2
·Microbiology
ESTEEM STERILE POLYISOPRENE SURGICAL GLOVES
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
PF4 IGG
FDA Adverse Event
Malfunction
·IMMUCOR GTI DIAGNOSTICS·Product code GWG·January 16, 2015
ATTAIN ABILITY PLUS
FDA Adverse Event
Malfunction
·MPRI·Product code OJX·April 22, 2013
ASR UNI FEMORAL IMPL SIZE 49
FDA Adverse Event
Injury
·DEPUY INTL., LTD.·Product code KWA·April 15, 2011
RF 3000 GENERATOR
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code GEI·July 9, 2008
REVITAN, PROXIMAL PART, CONICAL, UNCEMENTED, 75, TAPER 12/14
FDA Adverse Event
Malfunction
·ZIMMER GMBH·Product code LZO·April 26, 2019
REVITAN, DISTAL PART, STRAIGHT, UNCEMENTED, 18/260
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·May 6, 2019
REVITAN, DISTAL PART, STRAIGHT, UNCEMENTED, 18/140
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·April 29, 2019
REVITAN, DISTAL PART, STRAIGHT, UNCEMENTED, 26/260
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·April 26, 2019
REVITAN, PROXIMAL PART, CYLINDRICAL, UNCEMENTED, 65, TAPER 12/14
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·April 29, 2019
REVITAN, DISTAL PART, CURVED, UNCEMENTED, 20/200
FDA Adverse Event
Malfunction
·ZIMMER GMBH·Product code KWA·February 13, 2019
REVITAN, DISTAL PART, STRAIGHT, UNCEMENTED, 20/140
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·August 7, 2018
OPTAN, STEM, RIGHT, UNCEMENTED, 16, TAPER 12/14
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code LZO·June 4, 2018
DREAMSTATION CPAP
FDA Adverse Event
Injury
·RESPIRONICS, INC·Product code BZD·November 22, 2021
REVITAN DIST. CURVED 16/200
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·October 5, 2018
UNKNOWN REVITAN DISTAL STEM
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·April 23, 2019
REVITAN®, DISTAL PART, CURVED, UNCEMENTED, 22/200
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·April 24, 2019
REVITAN DISTAL STEM HIP IMPLANT
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·April 24, 2019