11 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OTOVENT
FDA 510(k)
FDA Unclassified
·Unknown
Clydesdale™ Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994972972·CAGE 2920840 CLYDESDALE 22 0 DEG 8X40
CLYDESDALE PTC™ Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169190863·CAGE 4920840 CDALE PTC 22MM 0 DEG 8X40
Liofilchem MTS (MIC Test Strip)
FDA UDI
LIOFILCHEM SRL·18055182870094·
i-ED COIL
FDA UDI
KANEKA CORPORATION·04540778177154·The i-ED COIL is used for vascular embolization...
Instrument Case
FDA UDI
KATENA PRODUCTS, INC.·00841668110997·DOUBLE PLASTIC STERILIZATION CASE
VITAL SCIENTIFIC PT WITH CALCIUM
FDA 510(k)
FDA Class 2
·Hematology
LEXUS CERVICAL INTERVERTEBRAL BODY FUSION CAGE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ATLANTIS¿ SR PRO²
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - FREMONT (SUD)·Product code DQO·January 17, 2013
VIRTUOSO DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code LWS·December 13, 2010
530G INSULIN PUMP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·July 8, 2014