22 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LORENZ LACTOSORB LARYNGOTRACHEAL RECONSTRUCTION IMPLANTS
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
Zirlux
FDA UDI
HENRY SCHEIN, INC.·H65890124090·Zirlux Shading Liquid - Effects, orange, 30ml
TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648154270·TREK Coronary Dilatation Catheter 3.50 mm x 20 ...
TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648154232·TREK Coronary Dilatation Catheter 3.50 mm x 6 m...
TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648154263·TREK Coronary Dilatation Catheter 3.50 mm x 15 ...
TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648154249·TREK Coronary Dilatation Catheter 3.50 mm x 8mm...
TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648154256·TREK Coronary Dilatation Catheter 3.50 mm x 12 ...
TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648154294·TREK Coronary Dilatation Catheter 3.50 mm x 30 ...
TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648154287·TREK Coronary Dilatation Catheter 3.50 mm x 25 ...
ID NOW COVID-19
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH INC.·Product code QJR·December 15, 2020
Navagio
FDA UDI
Kalitec Direct LLC·B07330K0134090·Trial, TLIF, 27L OB STR 7Deg, 9mm
Battalion
FDA UDI
ALPHATEC SPINE, INC.·00840967187051·Battalion, LLIF Trial, 8°, 24 mm Wide, 09 mm X ...
CBC-SF
FDA 510(k)
FDA Class 2
·Hematology
MAXONE, BLOOD, BLOOD PRODUCTS AND IV FLUID WARMER
FDA 510(k)
FDA Class 2
·General Hospital
ID NOW COVID-19
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·January 7, 2021
DESARA
FDA Adverse Event
Injury
·CALDERA MEDICAL, INC.·Product code PAH·March 7, 2013
PRECISION XTRA
FDA Adverse Event
Malfunction
·Product code NBW·March 9, 2011
COATED VICRYL PLUS ANTIBACTERIAL SUTURE
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code GAM·March 11, 2008
GMK-SPHERE FEMORAL COMPONENT SPHERE CEMENTED SIZE 6+ R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·September 9, 2022
Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone
FDA Enforcement
Class II
·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012