149 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Massage Therapy Concepts
FDA UDI
Nysale, Inc·00850660004012·
MINRAD INC. NASAL SCAVENGING CIRCUIT
FDA 510(k)
FDA Class 2
·Anesthesiology
MOSS TUBES, INC. NASAL TUBE - MARK IV
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ESOPHYX Z+
FDA Adverse Event
Malfunction
·ENDOGASTRIC SOLUTIONS, INC.·Product code ODE·December 9, 2020
CARENDO
FDA Adverse Event
Other
·ARJO HOSPITAL EQUIPMENT AB·Product code FSA·August 8, 2012
INFUSOMAT SPACE
FDA Adverse Event
Malfunction
·B. BRAUN MELSUNGEN AG·Product code FRN·September 30, 2016
DW ARTHROSCOPY FLUID MANAGEMENT DEV
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HRX·June 19, 2024
INFUSOMAT SPACE
FDA Adverse Event
Malfunction
·B. BRAUN MELSUNGEN AG·Product code FRN·September 30, 2016
EXTERNAL SHEATH
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·May 6, 2024
FIBERTAK
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MBI·May 6, 2024
FOREFOOT IB IMPLANT SYS, PEEK
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HWC·June 7, 2024
TYSHAK II
FDA Adverse Event
Other
·B. BRAUN MEDICAL, INC.·Product code DQY·November 16, 2006
TIGHTROPE® II ABS, IMPLANT OPEN
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MBI·June 19, 2024
TIGHTROPE® II RT, RECON IB¿
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MBI·April 25, 2024
DYNANITE® STAPLE DRILL BIT, CAL, 2.0
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HTW·May 23, 2024
LNT IMPLANT SYSTEM, 4.75 BC SWIVELOCK
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MAI·June 10, 2024
NANO CORKSCREW FT, TI, W 3-0 FW
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MBI·May 6, 2024
MAMMOMARK
FDA Adverse Event
Malfunction
·DEVICOR MEDICAL PRODUCTS, INC·Product code NEU·February 6, 2020
EB EXC GRN 30IN 2-0 S/A SH
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code GAT·September 4, 2024
EB EXC GRN 30IN 2-0 S/A SH
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code GAT·September 4, 2024