137 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RK EPIDURAL NEEDLE
FDA 510(k)
FDA Class 2
·Anesthesiology
Vial Adaptor
FDA UDI
WEST PHARMA. SERVICES IL, . LTD·07290108240450·VA 20mm ML VF-USA
Cook
FDA UDI
COOK INCORPORATED·00827002141773·Fascial Dilator
Paltop
FDA UDI
PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108692389·Conical 5mm Straight Ball Abutment Ti
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0120050·Screw Sizing Block
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197175197·Coakley Curettes Fig. 5
170mm,...
OsteoMed
FDA UDI
OSTEOMED LLC·00845694034654·MFx Instrumentation Tray 3
MODIFICATION TO ALARMVIEW WIRELESS DATA NETWORK SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
BOLUSPRO ULTRA
FDA 510(k)
FDA Class 2
·Radiology
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·June 7, 2018
IAB : 8 FR - 40 CC
FDA Adverse Event
Injury
·ARROW INTERNATIONAL, INC.·Product code DSP·July 29, 2005
NAIL, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES SELZACH·Product code JDS·February 13, 2017
MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·July 14, 2005
UNKNOWN ENDURON LINER
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JDI·August 4, 2005
NIPRO
FDA Adverse Event
Other
·NIPRO MEDICAL CORPORATION.·Product code FIB·August 15, 2005
CONTAK RENEWAL 3
FDA Adverse Event
Death
·CLONMEL·Product code NIK·March 3, 2006
MULTI-LINK MINI VISION RX CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·GUIDANT VASCULAR INTERVENTION·Product code MAF·November 1, 2005
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR LTD.·Product code MCM·October 13, 2005
RUGEL (BARD/DAVOL)
FDA Adverse Event
Injury
·DAVOL·Product code FTL·September 14, 2005
IQ MARKER GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code DQX·August 4, 2005