745 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EMG BLUE NITRILE MEDICAL EXAMINATION GLOVE WITH CHEMOTHERAPY DRUG LABELING CLAIM
FDA 510(k)
FDA Class 1
·General Hospital
Oticon
FDA UDI
Oticon A/S·05707131271518·NERA PRO, KIT 10 WL OMNI 75 PB BE
REUSABLE STERILCONTAINER FILTER MODEL #JK090
FDA 510(k)
FDA Class 2
·General Hospital
INQUIRY AFOCUSII DIAGNOSTIC CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
Matrixx System
FDA UDI
NEXXT SPINE, LLC·00889929034705·Corpectomy, 14Dx16Wx23H 6°
Matrixx System
FDA UDI
NEXXT SPINE, LLC·00889929043110·Corpectomy, 14Dx16Wx23H 0°
ZEVO ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWQ·October 23, 2019
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
ZEVO ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWQ·December 19, 2018
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 IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013
MEDISENSE OPTIUM
FDA Adverse Event
Malfunction
·Product code NBW·June 27, 2011
VAIL BED
FDA Adverse Event
Injury
·Product code FMS·August 29, 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