17 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Sysmex Automated Blood Coagulation Analyzer CS-5100
FDA 510(k)
FDA Class 2
·Hematology
ECG Module(AHA)
FDA UDI
SAMSUNG MEDISON CO., LTD.·08806167712532·
Oticon
FDA UDI
Oticon A/S·05707131281043·NERA2 PRO, MINIBTE 312 WL 85 TC
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100554·LIEBERMAN SPECULUM SOLID LARGE
HNM Women Care
FDA UDI
HNM STAINLESS, LLC.·00812171027720·PESSARY, CUBE #7, W/DRAINS, 56mm
BD SYRINGE LUER-LOK¿ TIP
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·October 19, 2018
BD SYRINGE LUER-LOK¿ TIP
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·April 16, 2018
BD SYRINGE LUER-LOK¿ TIP
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·September 24, 2018
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code NKB·July 21, 2017
SUPRA SCAN DELIVERY SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MOTIFMESH SOFT TISSUE PATCH
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BD SYRINGE LUER-LOK¿ TIP
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·July 20, 2018
ANEURX
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR·Product code MIH·June 6, 2013
INFINITI VISION SYSTEM OZIL
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·June 22, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 8, 2014
1213809-2018-00553
FDA Adverse Event
Malfunction
·August 22, 2018
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code NKB·April 19, 2019