7 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Megadyne Patient Return Electrode Pad - Universal Dual (model 0846), Megadyne Patient Return Electrode Pad - Universal Plus (model 0847), Megadyne Patient Return Electrode Pad - Universal Dual Plus (model 0848)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ELMED INCORPORATED
FDA UDI
ELMED INCORPORATED·00198506086663·Curved Femoral Head Impactor, Overall Length: 7...
SYNGO.VIA MI WORKFLOWS
FDA 510(k)
FDA Class 2
·Radiology
ENDOBOY
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
UNKNOWN SUTURE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code GAN·November 14, 2008
OT VERIO PRO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 2, 2011
ACCU-CHEK ® ULTRAFLEX INFUSION SET
FDA Adverse Event
Injury
·ROCHE HEALTH SOLUTIONS INC·Product code FPA·July 18, 2013