7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HORIZON PUMP Y-TYPE BLOOD SET
FDA 510(k)
FDA Class 2
·General Hospital
Packout-5 - Class A First Aid Kit - Poly
FDA UDI
Certified Safety Manufacturing, Inc.·00766588226378·Packout-5 - Class A First Aid Kit - Poly
LITE DECOMPRESSION SYSTEM- LIGHT CABLE MODEL 48089999
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BD-3000 MICROKERATOME SYSTEM, MODEL K-3000 MICROKERATOME
FDA 510(k)
FDA Class 1
·Ophthalmic
GYNECARE THERMACHOICE III
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code MKN·June 24, 2014
UNKNWON IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code EZW·January 18, 2013
PRECISION
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 12, 2010