9 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MODIFICATION TO X-PORT DUO PORT
FDA 510(k)
FDA Class 2
·General Hospital
Baltic Denture System BD Load
FDA UDI
Merz Dental GmbH·D7091034065·Baltic Denture System BD Load BDLoad ↓ Mm7 PLSE...
BD LUER-LOK¿ SYRINGE STERILE, SINGLE USE, 10 ML
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·June 7, 2022
WAKO NEFA LINEARITY SET
FDA 510(k)
FDA Class 1
·Clinical Chemistry
SOFT VENOUS RESERVOIR (SVRXX) WITH GBS COATING
FDA 510(k)
FDA Class 2
·Cardiovascular
AU480 CLINICAL CHEMISTRY ANALYZER WITH ISE
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code JGS·April 3, 2013
UNKNOWN DEPUY ASR HIP
FDA Adverse Event
Injury
·DEPUY INTL, LTD.·Product code KWA·March 24, 2011
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·April 24, 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