154 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MagPro R20
FDA 510(k)
FDA Class 2
·Neurology
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776085803·Senning Vascular Suction
CoRoent
FDA UDI
Nuvasive, Inc.·00887517566782·CoRoent Ant TLIF PEEK, 16x10x28mm 0°
NA
FDA UDI
MAKO SURGICAL CORP.·00848486020590·ACETABULAR REAMER ¿ 61mm
3M™ Unitek™
FDA UDI
3M UNITEK CORPORATION·00652221045010·Unitek(TM) Molar Band General Purpose Narrow Re...
Denovo general purpose dental molar band
FDA UDI
Denovo Dental, Inc.·00810059290730·Denovo general purpose dental molar band - Mand...
Rumex
FDA UDI
RUMEX INTERNATIONAL CORP.·00840159910092·Corneal Trephine Blades, 5.50 mm
GYNCARE MORCELLEX TISSUE MORCELLATOR
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
ICHEM 100 URINE CHEMISTRY ANALYZER
FDA 510(k)
FDA Class 2
·Clinical Chemistry
CAPSURE FIX NOVUS
FDA Adverse Event
Malfunction
·MPRI·Product code DTB·June 10, 2013
SYNCHRON LX 20 PRO SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·June 2, 2011
COLLEAGUE CX VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 16, 2008
CAPIOX FX OXYGENATOR
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·October 15, 2024
CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·November 19, 2021
CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·November 19, 2021
OSSIX BONE, OSSIX PLUS
FDA Adverse Event
Injury
·DATUM DENTAL LTD.·Product code NPM·June 22, 2022
CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·November 19, 2021
CAPIOX FX25 OXYGENATOR
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·July 22, 2020
BALL HEADS: MECTACER HEAD BIOLOX OPTION Ø 28
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·August 20, 2024
CAPIOX FX05
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·April 21, 2020