10 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
BIOGEL SKINSENSE POWDER-FREE NON-LATEX SURGEON'S GLOVE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
PILLING
FDA UDI
TELEFLEX INCORPORATED·24026704506327·
JOBST forMen
FDA UDI
BSN MEDICAL, INC.·04042809844832·FOR MEN 20-30 MM HG KNEE HIGH CLOSED TOE LARGE ...
ENDO LINEAR CUTTERS-ECHELON 60MM
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GDW·June 13, 2006
PARE ENDOSCOPIC SUTURING SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
WIENER LAB. FER-COLOR TRANSFERRINA, MODEL AUX. REAGENTS FOR 25 SAMPLES CAT. 1492002
FDA 510(k)
FDA Class 1
·Clinical Chemistry
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI PLANT - ST. PAUL·Product code NVY·April 11, 2013
CONTAK RENEWAL
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·April 13, 2011
SHIELDED INSYTE AUTOGUARD
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FOZ·May 16, 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