31 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NobelDesign, DTX Studio Design
FDA 510(k)
FDA Class 2
·Dental
Vyaire
FDA UDI
Jaeger Medical GmbH·34250892904918·Vyntus SPIRO
Jaeger
FDA UDI
Jaeger Medical GmbH·34250892900781·Vyntus Spiro
Jaeger
FDA UDI
Jaeger Medical GmbH·34250892900835·Vyntus Spiro
Vyaire
FDA UDI
Jaeger Medical GmbH·34250892904925·Vyntus SPIRO
Jaeger
FDA UDI
Jaeger Medical GmbH·34250892908633·Vyntus SPIRO
DCA VANTAGE, MODEL 5075
FDA 510(k)
FDA Class 2
·Hematology
GUIDEMIA
FDA 510(k)
FDA Class 2
·Radiology
BIZACT
FDA Adverse Event
Injury
·COVIDIEN MFG DC BOULDER·Product code GEI·June 18, 2019
STIMQ PERIPHERAL NERVE STIMULATOR (PNS) SYSTEM
FDA Adverse Event
Injury
·STIMWAVE TECHNOLOGIES INC.·Product code GZF·December 20, 2018
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 15, 2013
GREENLIGHT MOXY
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·June 30, 2011
PROLIEVE THERMODILITATION SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code MEQ·September 17, 2008
EA DELTA CER INSERT 36IDX52OD
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS INC US·Product code LZO·March 4, 2021
BIZACT
FDA Adverse Event
Malfunction
·COVIDIEN MFG DC BOULDER·Product code GEI·April 30, 2024
STIMQ PERIPHERAL NERVE STIMULATOR (PNS) SYSTEM
FDA Adverse Event
Injury
·STIMWAVE TECHNOLOGIES INC.·Product code GZF·April 1, 2019
BIZACT
FDA Adverse Event
Malfunction
·COVIDIEN MFG DC BOULDER·Product code GEI·April 30, 2024
BIZACT
FDA Adverse Event
Injury
·COVIDIEN MFG DC BOULDER·Product code GEI·October 19, 2020
BIZACT
FDA Adverse Event
Injury
·COVIDIEN MFG DC BOULDER·Product code GEI·October 19, 2020
BIZACT
FDA Adverse Event
Injury
·COVIDIEN MFG DC BOULDER·Product code GEI·October 19, 2020