634 results
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34ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SYNTHES LOW PROFILE NEURO SYSTEM
FDA 510(k)
FDA Class 2
·Dental
OsteoMed
FDA UDI
OSTEOMED LLC·00845694008051·2.0mm x 12mm Lag Screw
EVOS Lumbar Interbody System
FDA UDI
Cutting Edge Spine, LLC·00841193107110·HA PEEK EVOS Straight, ,12mmx9mmx 22mm , BICONV...
OsteoMed
FDA UDI
OSTEOMED LLC·00845694000369·2.0mm x 12mm Screw
OsteoMed
FDA UDI
OSTEOMED LLC·00845694034838·2.0 x 12mm Lag Screw, Sterile
OsteoMed
FDA UDI
OSTEOMED LLC·00845694028769·2.0mm x 12mm Screw, Sterile
OsteoMed
FDA UDI
OSTEOMED LLC·00845694054331·2.0 x 12mm Screw Sterile Qty 10
OsteoMed
FDA UDI
OSTEOMED LLC·00845694066488·HPS 2.0 x 12mm Lag Screw Sterile Qty 5
SYNTHETIC POWDERED (YELLOW) VINYL PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
ECG HOME
FDA 510(k)
FDA Class 2
·Cardiovascular
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·February 29, 2012
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·March 26, 2013
SM304 M-SERIES W/ZOOM
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code INK·March 10, 2011
TUBE, GASTROINTESTINAL (AND ACCESS)
FDA Adverse Event
Injury
·C.R. BARD, INC. (BASD)·Product code KNT·March 31, 2008
ALARIS PCA MODULE
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·October 26, 2020
ACRYSOF IQ TORIC
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·July 27, 2012
SKIN PREP 4.25OZ SPR
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code NEC·December 16, 2015
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·April 27, 2012
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR LTD·Product code MCM·November 2, 2012
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM INC.·Product code MDS·March 28, 2014