12 results
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34ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Indigo Aspiration System - Aspiration Catheter 12 and Separator 12
FDA 510(k)
FDA Class 2
·Cardiovascular
Mid America Energy - 18 Metal
FDA UDI
Certified Safety Manufacturing, Inc.·00766588082219·Mid America Energy - 18 Metal
DISCOVRED
FDA 510(k)
FDA Class 2
·Dental
ARAGON WIRING SYSTEM WIRE CARTRIDGE, MODELS I0007 WIRE CARTRIDGE, 22 GAUGE, I0008 WIRE CARTRIDGE, 24 GAUGE, I0009 WIRE E
FDA 510(k)
FDA Class 2
·Dental
ACCU-CHEK ULTRAFLEX INFUSION SET
FDA Adverse Event
Injury
·DISETRONIC MEDICAL SYSTEMS·Product code FPA·October 14, 2008
CAPSUREFIX NOVUS
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2011
ACCU-CHEK ® MULTICLIX
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·July 2, 2013
PERCUTANEOUS NEPHROSTOMY SET WITH SIMPLE LOOP VORTEK CATHETER
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code LJE·November 22, 2024
PERCUTANEOUS NEPHROSTOMY SET WITH SIMPLE LOOP VORTEK CATHETER
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code LJE·November 22, 2024
PERCUTANEOUS NEPHROSTOMY SET WITH SIMPLE LOOP VORTEK CATHETER
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code LJE·November 22, 2024
PERCUTANEOUS NEPHROSTOMY SET WITH SIMPLE LOOP VORTEK CATHETER
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code LJE·November 22, 2024
Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone
FDA Enforcement
Class II
·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012