11 results
·
26ms
·
Sources: EU EUDAMED, US FDA
ENZYMUN TEST(R) FSH
FDA 510(k)
FDA Class 1
·Clinical Chemistry
Tray
FDA UDI
Biomet Orthopedics, LLC·00880304467194·
ARROW
FDA UDI
TELEFLEX INCORPORATED·10801902140873·Pediatric Two-Lumen Central Venous Catheterizat...
PX 53/15-BP, MODEL 130 050 AND PX 60/15-BP, MODEL 130 051
FDA 510(k)
FDA Class 3
·Cardiovascular
RESTORIS MULTICOMPARTMENTAL KNEE (MCK) SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·June 27, 2014
INFUSOR TWO DAY 2ML/HR 12 PK
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·November 16, 2010
COYOTE¿ ES
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LIT·January 8, 2013
RECIPROC BLUE FILES, 6X, STERILE
FDA Adverse Event
Malfunction
·VDW GMBH·Product code EKS·July 29, 2025
RECIPROC BLUE FILES, 6X, STERILE
FDA Adverse Event
Malfunction
·VDW GMBH·Product code EKS·July 29, 2025
STEALTHSTATION¿ S8 SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code HAW·January 24, 2025