10 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IMC SURGICAL GOWNS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Ophthalmic Forceps
FDA UDI
KATENA PRODUCTS, INC.·00841668106334·SNIDER SUTURING FORCEPS 0.12MM
Expert
FDA UDI
C A I INDUSTRIES CORP·00807689005407·0.25x50mm acupuncture needles.
COAMATIC LR ANTITHROMBIN, NOTE: LR=LIQUID REAGENTS
FDA 510(k)
FDA Class 2
·Hematology
RDH BANDAGE
FDA 510(k)
FDA Class 1
·General Hospital
PEN NDL 32G 4MM PRO 100 BOX 1200 US
FDA Adverse Event
Malfunction
·BECTON DICKNSON AND CO. - DUN LAOGHAIRE CO, IRELAND·Product code FMI·February 6, 2024
ENDOTAK RELIANCE
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVY·April 11, 2013
IAB: 7.5 FR - 40 CC
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL INC·Product code DSP·May 22, 2008
PULSE GEN MODEL 103
FDA Adverse Event
Injury
·CYBERONICS, INC.·Product code LYJ·April 11, 2011
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