40 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DermaTherapy Bed Linens
FDA 510(k)
FDA Class 1
·General Hospital
STERRAD CYCLESURE 24 BIOLOGICAL INDICATOR
FDA 510(k)
FDA Class 2
·General Hospital
MODEL DFP-8000D/FPD DIGITAL RADIOGRAPHY SYSTEM WITH FLAT PANEL DETECTOR
FDA 510(k)
FDA Class 2
·Radiology
UNKNOWN PATHINDER NXT OR INSTINCT JAVA IMPLANT
FDA Adverse Event
Malfunction
·ZIMMER BIOMET SPINE INC.·Product code NKB·September 24, 2022
BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B LABORATORY KIT
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·March 3, 2026
ATTAIN LV
FDA Adverse Event
Injury
·MPRI·Product code LWP·June 8, 2013
ACUITY CENTRAL MONITORING
FDA Adverse Event
Malfunction
·WELCH ALLYN PROTOCOL, INC.·Product code DSI·June 28, 2011
GE OEC 9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 10, 2008
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 24, 2024
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 24, 2024
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 25, 2024
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 24, 2024
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 24, 2024
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 24, 2024
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 24, 2024
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 24, 2024
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 25, 2024
MERGE HEMO
FDA Adverse Event
Malfunction
·MERGE HEALTHCARE·Product code DQK·September 24, 2024
BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B LABORATORY KIT
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·October 7, 2025
BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B LABORATORY KIT
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·February 24, 2026