18 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Lens, Contact (Other Material) - Daily
FDA Pre-Market Approval
FDA Class 2
·PARAPERM O2 CLEAR & BLUE LENS
PressON™
FDA UDI
NEXUS SPINE, L.L.C.·B6788200620·External Pedicle Driver
Monitor, Intracranial Pressure, Implanted
FDA Pre-Market Approval
FDA Class 3
·COSMAN ICP TELE-SENSOR(R)
Separator, Automated, Blood Cell And Plasma, Therapeutic
FDA Pre-Market Approval
FDA Unclassified
·CRYOMAX(TM)
DISPOSABLE PLASTIC SYRINGE & NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
Monitor, Intracranial Pressure, Implanted
FDA Pre-Market Approval
FDA Class 3
·COSMAN ICP TELE-SENSOR(R)
Monitor, Intracranial Pressure, Implanted
FDA Pre-Market Approval
FDA Class 3
·ICP TELE-MONITOR & ICP TELE-SENSOR
Separator, Automated, Blood Cell And Plasma, Therapeutic
FDA Pre-Market Approval
FDA Unclassified
·CRYOMAX(TM)
Separator, Automated, Blood Cell And Plasma, Therapeutic
FDA Pre-Market Approval
FDA Unclassified
·CRYOMAX(TM)
Monitor, Intracranial Pressure, Implanted
FDA Pre-Market Approval
FDA Class 3
·COSMAN ICP TELE-SENSOR(R) & COSMAN
Monitor, Intracranial Pressure, Implanted
FDA Pre-Market Approval
FDA Class 3
·COSMAN ICP TELE-SENSOR(R)
Monitor, Intracranial Pressure, Implanted
FDA Pre-Market Approval
FDA Class 3
·COSMAN ICP TELE-SENSOR(R)
3.5MM LCP® PROXIMAL HUMERUS PLATE-STANDARD 5H SHAFT/114MM
FDA Adverse Event
Injury
·SYNTHES USA·Product code KTW·May 20, 2014
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code FSA·November 5, 2012
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 23, 2010
BINAXNOW STREP PNEUMONIAE 12T
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code GTZ·March 27, 2025
BINAXNOW STREP PNEUMONIAE 12T
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code GTZ·March 27, 2025
BINAXNOW STREP PNEUMONIAE 12T
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code GTZ·March 27, 2025