7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ELECTRO-NERVE STIMULATOR TENS MODEL MICRO PLUS-A
FDA 510(k)
FDA Class 2
·Neurology
MATIRA ANTERIOR CERVICAL SYSTEM
FDA UDI
Kalitec Direct LLC·B07307K0152100·Handle, Guide, Offset Angled
PHONAK 9800 SC-AF ITE HEARING INSTRUMENT
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
SLIDEX MENINGITE-KIT 5
FDA 510(k)
FDA Class 2
·Microbiology
PLUM A+ DRIVER ED 2
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·May 16, 2014
DA VINCI SURGICAL SYSTEM
FDA Adverse Event
Other
·INTUITIVE SURGICAL,INC.·Product code NAY·December 6, 2010
HEARTSINE SAMARITAN 300P AND PAD PAK
FDA Adverse Event
Malfunction
·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·December 19, 2012