7 results
·
19ms
·
Sources: EU EUDAMED, US FDA
RESILIENT GUM EXERCISER
FDA 510(k)
FDA Class 1
·Dental
Unipack
FDA UDI
UNIPACK MEDICAL CORPORATION·D784UBC8209791·X-Ray Sensor Sheaths Carestream/Kodak 6100, Size 2
CAREFUSION NICOLET EDX
FDA 510(k)
FDA Class 2
·Neurology
SYSMEX AUTOMATED COAGULATION ANALYZER, MODEL #CA-7000
FDA 510(k)
FDA Class 2
·Hematology
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 8, 2014
ACCU-CHEK ® COMPACT TEST DRUM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·November 6, 2012
ENDOPOUCH RETRIEVER SPEC BAG
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GCJ·October 9, 2007