54 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
NMI PICC III and NMI PICC IV
FDA 510(k)
FDA Class 2
·General Hospital
ECG Module(AHA)
FDA UDI
SAMSUNG MEDISON CO., LTD.·08806167712532·
Oticon
FDA UDI
Oticon A/S·05707131288936·H11V2 TI, RITE 312 WL CBE
OSS™ Orthopedic Salvage System
FDA UDI
Biomet Orthopedics, LLC·00880304239692·
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100127·KRATZ-BARRAQUER SPECULUM RIGHT EYE
Patella Drill Guide
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215074166·
CHROMOPEP PC, CHROMOPEP AT, MODELS 2.5 AND 5
FDA 510(k)
FDA Class 2
·Hematology
ASCENSION MODULAR TOTAL SHOULDER SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
VERSYS FEMORAL STEM
FDA Adverse Event
Injury
·ZIMMER INC·Product code LPH·February 25, 2016
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
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Injury
·ANIMAS CORPORATION·Product code LZG·June 6, 2013
PIRANHA 3F URETEROSCOPIC BIOPSY DEVICE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FCL·August 21, 2008
PERCUTANEOUS INTRASPINAL CATHETER KIT
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·September 5, 2008
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
INSPIRE 8F
FDA Adverse Event
Injury
·SORIN GROUP ITALIA·Product code DTZ·November 5, 2025
INSPIRE OXYGENATOR
FDA Adverse Event
Injury
·SORIN GROUP ITALIA·Product code DTZ·December 11, 2025