9 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ULTRASHARP CONCENTRIC NEEDLES
FDA 510(k)
FDA Class 2
·Physical Medicine
SchureMed
FDA UDI
SCHUERCH CORPORATION·00810014608273·ALLEN, STERIS-AMSCO 4" DELUXE
BEAUTIFIL
FDA 510(k)
FDA Class 2
·Dental
ACTALYKE XL ACTIVATED CLOTTING TIME ANALYZER, MODEL 5770
FDA 510(k)
FDA Class 2
·Hematology
WAVEWRITER ALPHA
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·April 21, 2023
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FKX·April 26, 2013
UNICEL® DXC 800 PRO SYNCHRON® CHEMISTRY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·May 7, 2011
TROCH ENTRY NAIL RH 9MMX32CM
FDA Adverse Event
Injury
·DEPUY ACE S.A. 'R.L.·Product code HSB·July 22, 2008
Natrelle 133 Series Tissue Expanders Product Usage: Natrelle 133 Series Tissue Expander is intended for temporary subcutaneous implantation and require periodic, incremental inflation with sterile saline for injection until the desired amount of tissue is developed.
FDA Enforcement
Class II
·Terminated·Allergan Inc·July 29, 2015