29 results
·
57ms
·
Sources: EU EUDAMED, US FDA
CELL-DYN 22 Plus Calibrator
FDA registration
STRECK LLC·1 product·🇺🇸 United States
Chartis Console
FDA registration
PULMONX, Corp.·1 product·🇺🇸 United States
Summa Orthopaedics System Surgical Instrument
FDA UDI
Jeil Medical Corporation·08800089402687·
MESH URETERAL STENT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
TEMPUS IC PROFESSIONAL PATIENT MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
Intervertebral Fusion Device With Bone Graft, Cervical
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Cervical
111-301
FDA registration
JEIL MEDICAL CORPORATION·1 product·🇰🇷 South Korea
Stent, Ureteral
FDA classification
FDA Class 2
·Stent, Ureteral
Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
FDA classification
FDA Class 2
·Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)