747 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SMARTDOP XT
FDA 510(k)
FDA Class 2
·Cardiovascular
CoRoent
FDA UDI
Nuvasive, Inc.·00887517597298·CoRoent Large MP Ti, 16x9x23mm 12°
OsteoMed
FDA UDI
OSTEOMED LLC·00845694043731·LPM Mesh, 187mm x 161mm x 0.6mm
Phantom® Fibula Nail System
FDA UDI
Paragon 28, Inc.·00889795137128·1.6mm x 230mm, Sterilization K-Wire Container
MODIFICATION TO COALESCENT SURGICAL U-CLIP AND ACCESSORIES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
INQUIRY AFOCUSII DIAGNOSTIC CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 12, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 11, 2024
BIPAP A40
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 9, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 6, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 13, 2024
OT VERIO PRO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013
PERCLOSE A-T SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·June 16, 2011
30327 12CC 100 UNIT HEP SYR {CAN} (5CC)
FDA Adverse Event
Malfunction
·TYCO HEALTHCARE/KENDALL·Product code NZW·August 21, 2008
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 16, 2024
BIPAP A40 PRO, IT
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 5, 2025
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·June 5, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·June 6, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·June 5, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 11, 2024