16 results
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37ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ISCHEMA VIEW RAPID
FDA 510(k)
FDA Class 2
·Radiology
MaxFuse VBR, 10 (D) x 12 (W) x 56 (H)
FDA UDI
Pioneer Surgical Technology, Inc.·00846468055677·VBR, 10 (D) x 12 (W) x 56 (H)
BD LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·July 10, 2025
LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·July 10, 2025
TELE-CLINIQ DATA TRANSMISSION SYSTEM BLOOD PRESSURE MEASUREMENT SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
ZIMMER PERIARTICULAR SCREWS
FDA 510(k)
FDA Class 2
·Orthopedic
Matrixx System
FDA UDI
NEXXT SPINE, LLC·00889929038895·Corpectomy, 12Dx14Wx47H 6°
Matrixx System
FDA UDI
NEXXT SPINE, LLC·00889929064818·Corpectomy, 12Dx14Wx47H 0°
GMK PRIMARY FIXED CEMENTED FEMUR SIZE 5 LEFT
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL, SA·Product code JWH·July 18, 2013
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013
INFINITI VISION SYSTEM OZIL
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·July 29, 2014
CLEO 90 INFUSION SET
FDA Adverse Event
Malfunction
·SMITHS MEDICAL·Product code FPA·May 6, 2011
AXIUM
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 10, 2019
AXIUM
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 10, 2019
AXIUM
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 10, 2019
AXIUM
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 11, 2019