11 results
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21ms
·
Sources: EU EUDAMED, US FDA
LABELING CHANGE - VIASPAN(TM) (BELZER UW)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SOMATEX
FDA UDI
BIOPSYBELL SRL·08033860021818·
DELTRAN
FDA UDI
UTAH MEDICAL PRODUCTS, INC.·H6719004920·DELTRAN II, Pressure Monitoring Kit, 3cc/hr Flo...
1.5MM SMALL LOCKING PLATE, 1.5MM NON-LOCKING AND LOCKING SCREWS
FDA 510(k)
FDA Class 2
·Orthopedic
MDA D-DIMER
FDA 510(k)
FDA Class 2
·Hematology
SOLYX SIS SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PAH·October 1, 2020
PINN MAR +4 NEUT 36IDX52OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·June 27, 2014
ACCU-CHEK ® COMPACT TEST DRUM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·January 7, 2013
WECK HEMOLOK ENDO APPLIER 5MM
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code FZP·October 29, 2010
SOLYX SIS SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code PAH·October 1, 2020
STEALTHSTATION¿ S8 SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code HAW·September 12, 2023