10 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ARGYLE CONNECT TUBE-CON & NON
FDA 510(k)
FDA Class 2
·General Hospital
ACUMED
FDA UDI
Acumed LLC·10806378105159·Small Frag 2-Level Case Base
VACUETTE WITH PPACK
FDA 510(k)
FDA Class 2
·Clinical Chemistry
TWISTCUT ENDOSORB SCREWS
FDA 510(k)
FDA Class 2
·Orthopedic
PLUM 1.6 W/DATAPORT
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·February 21, 2014
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·October 1, 2007
UNKNOWN DEPUY SROM HIP LINER
FDA Adverse Event
Injury
·DEPUY RAYNHAM·Product code JDI·October 24, 2012
EVOLUT FX PLUS VALVE
FDA Adverse Event
Malfunction
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·March 3, 2025
ACUSON Sequoia Ultrasound Imaging System with Software Version VA25A/B
FDA Enforcement
Class II
·Ongoing·Siemens Medical Solutions USA, Inc.·February 9, 2022
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