38 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ZOLL E SERIES ALS
FDA 510(k)
FDA Class 2
·Cardiovascular
LOCATOR R-Tx
FDA UDI
Zest Anchors, LLC·00840481120862·LOCATOR R-Tx Abutment For UF(II) Narrow Platfor...
BONNEY TISSUE FORCEPS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896023901·BONNEY TISSUE FORCEPS TUNGSTEN CARBIDE SERRATED...
n/a
FDA UDI
Ortho Development Corporation·00822409067107·Stem Trial 14x50mm
ASCENSION TOTAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SONOLINE EBISU DIAGNOSTIC ULTRASOUND SYSTEMS
FDA 510(k)
FDA Class 2
·Radiology
Specials
FDA UDI
Seaspine Orthopedics Corporation·10889981440855·Drill, 12mm
Specials
FDA UDI
Seaspine Orthopedics Corporation·10889981440879·Drill, 14mm
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·December 27, 2021
MONOJECT
FDA Adverse Event
Malfunction
·JIANGSU CAINA MEDICAL CO., LTD·Product code PNR·April 14, 2024
CARDINAL HEALTH
FDA Adverse Event
Malfunction
·JIANGSU CAINA MEDICAL CO., LTD.·Product code PNR·April 12, 2024
CARDINAL
FDA Adverse Event
Malfunction
·JIANGSU CAINA MEDICAL CO., LTD.·Product code PNR·April 12, 2024
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·August 9, 2021
LOGIC FEMORAL PS POR RIGHT SZ 2
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·February 10, 2025
VIAL-MATE RECONSTITUTION DEVICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code LHI·January 10, 2022
HAKIM VLAVE
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC.·Product code JXG·May 31, 2013
ALLSCRIPTS PRO EHR
FDA Adverse Event
Malfunction
·ALLSCRIPTS SOLUTIONS·Product code JQP·June 21, 2011
INSIGNIA
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 3, 2014
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·November 19, 2021
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·June 2, 2021