39 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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CHEVEUX DIODE LASER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Endo Carry-On Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964061530·Endo Carry-on Procedure Kit includes 5-piece Ol...
MODIFICATION TO HYBRID CAPTURE 2 GC-ID DNA TEST, MODEL 03M92-01
FDA 510(k)
FDA Class 2
·Microbiology
AC POWERED THERMAL CAUTERY UNIT
FDA 510(k)
FDA Class 2
·Ophthalmic
BD VACUTAINER SERUM BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·January 21, 2021
Widex
FDA UDI
Widex A/S·05706069773569·Widex EVOKE E-FA (Lime Green S-330 ) Telecoil, ...
BD VACUTAINER SERUM BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·June 16, 2021
STEALTHSTATION® S7¿
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code HAW·April 19, 2023
11.0MM TI HELICAL BLADE 100MM-STERILE
FDA Adverse Event
Injury
·SYNTHES ELMIRA·Product code HSB·May 12, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 8, 2013
GYNECARE TVT
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·September 19, 2014
ENDOPATH** ETS45
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·May 24, 2011
11.0MM TI HELICAL BLADE 95MM-STERILE
FDA Adverse Event
Malfunction
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HSB·December 17, 2018
BD VACUTAINER® EDTA 2K
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·June 15, 2018
BD VACUTAINER SERUM BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·March 22, 2021
BD VACUTAINER® SERUM BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·March 22, 2021
White
FDA UDI
COOK INCORPORATED·00827002280083·White Vessel Sizing
Cook
FDA UDI
COOK INCORPORATED·00827002472990·White Sizing Catheter
TherMax Blood Warmer Unit
FDA Enforcement
Class II
·Terminated·Baxter Healthcare Corporation·November 6, 2019
IVEA Product Part Number 16100 Model 500A
FDA Enforcement
Class II
·Terminated·Firefly Medical, Inc.·October 11, 2017