23 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NIPRO SAFETOUCH PSV SCALP VEIN SET WITH SAFETY DEVICE
FDA 510(k)
FDA Class 2
·General Hospital
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·00636257125168·20-30 MV FOR MEN CLSC CALF STD TAN VI
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·00636257127292·20-30 MV FOR MEN SEL CALF STD TAN VI
Fuji Cervical Plate System
FDA UDI
Altus Spine, LLC·B41711401361·36mm Level 1 Cervical Plate System - Fuji
Hayden Medical
FDA UDI
Hayden Medical, Inc.·00840319720639·Rochester (Pean) Hemostatic Forceps 5-1/2" (14c...
RESPICHAMBER VALVED HOLDING CHAMBER
FDA 510(k)
FDA Class 2
·Anesthesiology
EMBRYOGEN
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Widex
FDA UDI
Widex A/S·05706069923544·WIDEX MOMENT MBB3D 440 (Deep blue)
Widex
FDA UDI
Widex A/S·05706069972344·WIDEX MOMENT MBB2 440 (Deep blue)
Widex
FDA UDI
Widex A/S·05706069715705·Widex EVOKE E-FA (Deep Blue ) 440, Telecoil, Vo...
Widex
FDA UDI
Widex A/S·05706069718317·Widex EVOKE E-FM (Deep Blue ) 440, RC coil
Widex
FDA UDI
Widex A/S·05706069716054·Widex EVOKE E-FP (Deep Blue ) 440, Telecoil, Vo...
Widex
FDA UDI
Widex A/S·05706069884630·WIDEX MOMENT MRR2D (Deep Blue ) 440, RC coil, m...
ULTRAMINI
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·September 18, 2007
ENDO GIA ADAPTER XL
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GAG·October 3, 2014
VASO VIEW HEMOPRO
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC·Product code GEI·May 29, 2013
COLLEAGUE PRE-P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 25, 2011
ARCHITECT C16000 SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING INC·Product code JJE·June 26, 2019
ONE TOUCH ULTRAMINI METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·February 22, 2010
AQUAPAK 640 SW, 650ML W/040 ADAPTOR, INTL. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor packaged with the water bottle is affected by this recall.
FDA Enforcement
Class II
·Terminated·Teleflex Medical·February 18, 2015