11 results
·
26ms
·
Sources: EU EUDAMED, US FDA
HybridAPC probe
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MaXcess
FDA UDI
Nuvasive, Inc.·00887517198648·MaXcess 4 Blade, 120mm Electrode Ctr
Ophthalmic Cannula
FDA UDI
KATENA PRODUCTS, INC.·00841668113875·VISCO INJECTION CANNULA 30GA ANG 10MM
TAPERLOC COMPLETE RASP/PROVISIONAL
FDA UDI
Biomet Orthopedics, LLC·00880304632424·
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197046336·Titan Adson Brown Tissue Forceps
7x7 te...
MIN-FILTER/S, UNI-FILTER JUNIOR, UNI-FILTER/S ANGLED AND UNI-FILTER
FDA 510(k)
FDA Class 2
·Anesthesiology
OrthoPulse
FDA 510(k)
FDA Class 2
·Dental
CLINITEK STATUS+
FDA Adverse Event
SIEMENS HEALTHCARE DIAGNOSTICS·Product code JIL·May 16, 2016
PROMOTE ACCEL CRT-D
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·September 11, 2011
RESERVOIR 3ML
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·November 11, 2014
MAQUET SAS
FDA Adverse Event
Malfunction
·MAQUET SAS·Product code FSY·July 17, 2013