76 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Persyst 15 EEG Review and Analysis Software
FDA 510(k)
FDA Class 2
·Neurology
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690126461·Adjustable Modular Tibia Tray Trial Size 2
OTS - Class B 21 Field Trauma - Hawkespack
FDA UDI
Certified Safety Manufacturing, Inc.·00766588620022·OTS - Class B 21 Field Trauma - Hawkespack
pjur Original
FDA UDI
Pjur Group Luxembourg SA·00827160100773·Silicone-based Personal Lubricant
Synthetic Vinyl Examination Gloves
FDA 510(k)
FDA Class 1
·General Hospital
SYDNEY IVF CULTURE OIL
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024242838·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024242791·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024242814·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024242821·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024242807·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024242852·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024242845·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024242869·
SILHOUETTE
FDA Adverse Event
Malfunction
·MAERSK MEDICAL A/S·Product code FPA·December 11, 2002
QUICK SET PARADIGM
FDA Adverse Event
Malfunction
·MAERSK MEDICAL DEVICE S.A. DE C.V.·Product code FPA·December 11, 2002
SILHOUETTE
FDA Adverse Event
Malfunction
·MAERSK MEDICAL A/S·Product code FPA·December 11, 2002
QUICK SET PARADIGM
FDA Adverse Event
Malfunction
·MAERSK MEDICAL DEVICE S.A. DE C.V.·Product code FPA·December 11, 2002
SILHOUETTE
FDA Adverse Event
Malfunction
·MAERSK MEDICAL A/S·Product code FPA·December 6, 2002
SILHOUETTE
FDA Adverse Event
Malfunction
·MAERSK MEDICAL A/S·Product code FPA·December 6, 2002