8 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BD Kiestra IdentifA
FDA 510(k)
FDA Class 2
·Microbiology
BD KIESTRA IDENTIFA
FDA Adverse Event
Malfunction
·BD KIESTRA LAB AUTOMATION·Product code QBN·October 8, 2025
Oticon
FDA UDI
Oticon A/S·05707131340153·SIYA 2, KIT 312 NFM 75 R C001
AUDIT MICROCV URINE/FLUIDS CHEMISTRY LINEARITY
FDA 510(k)
FDA Class 1
·Clinical Chemistry
CREST GLIDE CLINICAL GUM PROTECTION DENTAL FLOSS
FDA 510(k)
FDA Class 1
·Dental
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE·Product code KDJ·August 4, 2011
LUPINE DRILL GUIDE
FDA Adverse Event
Malfunction
·DEPUY MITEK·Product code HRX·October 1, 2008
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 27, 2013