73 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ASCENSION MODULAR TOTAL SHOULDER SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ACE
FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950014163·MOUTH PROP EXACTA WITH 10MM PIN AUTOCLAVABLE
Bur PM2-95 80K Steel Ø2.3 St
FDA UDI
Bien-Air Surgery SA·17630055504033·
Bur PM2-95 80K steel Ø2.3mm sterile
FDA UDI
Bien-Air Surgery SA·J00711004480011·
Digital Analogue NP
FDA UDI
RP - CONEXOES RESTAURADORAS LTDA·07901059074772·
GEN4 INTERACTIVE
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828161961·GEN4 INTERACTIVE
GEN4 Direct Access
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828105538·GEN4 Direct Access
GEN4 DIGITAL
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828112352·GEN4 DIGITAL
PACSSTATION
FDA 510(k)
FDA Class 2
·Radiology
HORIZONS INTERNATIONAL VARICES INJECTION NEEDLES
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
INSPIRE 8F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA SRL·Product code DTZ·May 5, 2020
INSPIRE 8F M
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA·Product code DTZ·January 3, 2024
MERIT CONVENIENCE KIT
FDA Adverse Event
Malfunction
·MERIT MEDICAL SYSTEMS, INC.·Product code DQO·January 15, 2010
COAGUCHEK® XS SYSTEM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code GJS·May 8, 2013
AFFINITY HFO W/TRILLIUM 511T
FDA Adverse Event
Malfunction
·PERFUSION SYSTEMS·Product code DTZ·September 19, 2014
7700
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·May 13, 2011
INSPIRE 8F M
FDA Adverse Event
Injury
·SORIN GROUP ITALIA·Product code DTZ·January 4, 2024
INSPIRE OXYGENATOR
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA·Product code DTZ·March 12, 2026
INSPIRE OXYGENATOR
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA·Product code DTZ·March 12, 2026
INSPIRE 8F
FDA Adverse Event
Injury
·SORIN GROUP ITALIA·Product code DTZ·November 5, 2025