15 results
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28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Diamondback 360 Peripheral Orbital Atherectomy System
FDA 510(k)
FDA Class 2
·Cardiovascular
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197074346·Meyerding Hemi Laminectomy retractor
18cm l...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197074353·Meyerding Hemi Laminectomy retractor
18cm l...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197074315·Meyerding Hemi Laminectomy retractor
18cm l...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197074322·Meyerding Hemi Laminectomy retractor
18cm l...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197074407·Meyerding Hemi Laminectomy retractor
18cm l...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197074339·Meyerding Hemi Laminectomy retractor
18cm l...
QLAB QUANTIFICATION
FDA 510(k)
FDA Class 2
·Radiology
GELPOINT PATH
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 2, 2025
MOTO PARTIAL KNEE SYSTEM - MEDIAL
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code HSX·December 30, 2024
MOTO PARTIAL KNEE TIBIAL TRAY FIX CEMENTED S3 RM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code HSX·November 24, 2021
ENDURANT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·June 14, 2013
ACCU-CHEK ® COMPACT TEST DRUM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·July 21, 2011
PLUMSET-DUAL W/CON PP, CAP PORT & CLAVE
FDA Adverse Event
Malfunction
·HOSPIRA DE COSTA RICA LTD·Product code FPA·September 15, 2008