10 results
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22ms
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Sources: EU EUDAMED, US FDA
SALINUM, ORCLAIR
FDA 510(k)
FDA Unclassified
·Unknown
Inspire®SA 3D Printed Trabecular PEEK™ with HAFUSE®
FDA UDI
CURITEVA, INC.·B648C72430241481·30 (W) X 24 (D) X 14 (H) X 8° (A) STANDALONE AL...
BD LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·May 26, 2024
SELF-DRILLING RADIOGRAPHIC MARKER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
pHoenix ISE Reagents FOR Olympus AU Chemistry Systems
FDA 510(k)
FDA Class 2
·Clinical Chemistry
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·March 27, 2013
AQUALINE
FDA Adverse Event
Malfunction
·HAEMOTRONICS SPA·Product code FJK·March 18, 2011
EAGLE 4000
FDA Adverse Event
Malfunction
·GE HEALTHCARE·Product code MHX·March 20, 2008
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
The Spirit Select Bed, Model 5700 Spirit Plus /with high rail siderail option
FDA Enforcement
Class II
·Terminated·Stryker Medical Division of Stryker Corporation·November 21, 2018