10 results · 22ms · Sources: EU EUDAMED, US FDA

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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