13 results
·
30ms
·
Sources: EU EUDAMED, US FDA
IL TEST BARBITURATE, 35289
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Accu-Beam
FDA UDI
TRANSAMERICAN TECHNOLOGIES INTERNATIONAL·B1779204170·Re-usable fiberoptic handpiece for lasers.
17ga...
Instrument Case
FDA UDI
KATENA PRODUCTS, INC.·00841668110928·STERILIZING CASE SINGLE VR
Spectrum IQ Infusion System with Dose IQ Safety Software
FDA 510(k)
FDA Class 2
·General Hospital
#506 PORT. VITAL FUNCTIONS NEONATAL MON
FDA 510(k)
FDA Class 2
·Cardiovascular
SPECTRUM IQ INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·March 23, 2022
SPECTRUM IQ INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·June 13, 2022
SPECTRUM IQ INFUSION PUMP
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORPORATION·Product code FRN·May 25, 2022
COLLEAGUE CX VOLUMETRIC INFUSION PUMP SINGLE CHANNEL
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·December 10, 2010
VERITY DR
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC., CRMD·Product code LWP·July 8, 2014
POWER LOAD
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FPO·December 7, 2012
SPECTRUM IQ INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·June 16, 2022
KING LAD Flexible ClearSeal SINGLE USE, King Systems ETO Sterilie, 10 devices/case "Size 4 / Adult ClearSeal Flexible King LAD¿ Patient Size: 50-70kg " Product Usage: Laryngeal airway
FDA Enforcement
Class II
·Terminated·King Systems Corp.·November 28, 2012