9 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STERI-OSS TIODIZED SCREW
FDA 510(k)
FDA Class 2
·Dental
KODAK EKTASCAN IMAGE TRANSMISSION SYSTEM P1
FDA 510(k)
FDA Class 2
·Radiology
DYNAPULSE 200M
FDA 510(k)
FDA Class 2
·Cardiovascular
TRANSPAC TRIFURCATED MONITORING KIT, 60" TUBING, 3 3 ML FLUSH DEVICE, MICRODRIP
FDA Adverse Event
Malfunction
·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·September 15, 2020
TRANSPAC TRIFURCATED MONITORING KIT, 60" TUBING, 3 3 ML FLUSH DEVICE, MICRODRIP
FDA Adverse Event
Malfunction
·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·September 15, 2020
MAXIMO II CRT-D
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·February 15, 2013
PRECISION TEST STRIPS
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 20, 2011
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 29, 2014
8.0MM/4.2MM DRILL SLEEVE 200MM
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code FZX·November 14, 2022