14 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EDGE MEDICAL DISPENSING PIN
FDA 510(k)
FDA Class 2
·General Hospital
PAQ.210X300X250.MORTARA X-SCR
FDA UDI
AB MEDICA GROUP, S.A.·08428763009689·
WRIST FIT
FDA UDI
Stryker GmbH·00886385000121·Volar Plate Narrow, Left
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471123052·K-WIRE - DOUBLE TROCAR 1.0mm DIA x 75mm
Liofilchem MTS (MIC Test Strip)
FDA UDI
LIOFILCHEM SRL·08055182872862·MTS is a quantitative assay for determining the...
WAVELIGHT FS200 PATIENT INTERFACE 1505
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
EBI XFIX RAIL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
COLORADO 2 SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC INC.·Product code MNH·December 4, 2009
COLORADO II SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code MNH·May 19, 2017
COLORADO SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·October 17, 2016
PULSE GEN MODEL 102R
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·December 9, 2010
PRIMEADVANCED
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·January 17, 2013
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 9, 2014
COLORADO II SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC, INC.·Product code KWP·July 26, 2011