10 results · 28ms · Sources: EU EUDAMED, US FDA

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CORPAK GRASPING FORCEPS

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

AXSOS

FDA UDI
Stryker GmbH·07613154110704·Metal Base - Screw Rack

IMAGEGRID RADIOLOGY VIEWER SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

MODIFICATION TO DATASCOPE PROFILE 8FR. IAB, 34CC; MODIFICATION TO DATASCOPE PROFILE 8FR. IAB, 40CC

FDA 510(k)
FDA Class 2 ·Cardiovascular

SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·June 30, 2014

XCELA LOW PROFILE PORT

FDA Adverse Event
Malfunction ·PFM MEDICAL, INC·Product code LJT·October 29, 2010

TOTALCARE BED

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code FNL·November 29, 2012

WITTICH NITINOL STONE BASKET

FDA Adverse Event
Malfunction ·COOK INC·Product code LQR·February 20, 2019

WITTICH NITINOL STONE BASKET

FDA Adverse Event
Malfunction ·COOK INC·Product code LQR·February 20, 2019

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