7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DENTAL HANDPIECE AND ACCESSORY
FDA 510(k)
FDA Class 1
·Dental
GEN-PROBE APTIMA ASSAY FOR NEISSERIA GONORRHOEAE MODEL#1091
FDA 510(k)
FDA Class 2
·Microbiology
Health-e-Connect System with IDA
FDA 510(k)
FDA Class 2
·Anesthesiology
DRILL F.RADIOLUCENT TARGETING DEVICE SIDEWINDER Ø3,2 MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS-KIEL·Product code LXH·September 16, 2013
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·August 4, 2015
CQUR TACSHIELD
FDA Adverse Event
Injury
·ATRIUM MEDICAL CORP·Product code FTL·January 2, 2013
EXTENDEVAC W/COATED BLADE 10FT. TUBING HOLSTER
FDA Adverse Event
Malfunction
·DEROYAL INDUSTRIES, INC.·Product code GEI·March 6, 2014