55 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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Spectra Optia Apheresis System
FDA 510(k)
FDA Unclassified
·Unknown
Epredia
FDA UDI
SHANDON DIAGNOSTICS LIMITED·05051663517751·CTM6 coverslipper- Accessory
BR2000 BLADES
FDA UDI
Peter Brasseler Holdings, LLC·00887919100812·K7-2590-47
Brasseler
FDA UDI
Provision·B504OMK72590500·
Brasseler
FDA UDI
Provision·B504OMK72590470·
NA
FDA UDI
STERILMED, INC.·10888551007511·SAW BLADE OSCILLATING AGGRESSIVE CUT LARGE BONE
NA
FDA UDI
STERILMED, INC.·10888551007504·SAW BLADE OSCILLATING AGGRESSIVE CUT LARGE BONE
INSPIRATION; VENTILATOR SYSTEM, LS VENTILATOR SYSTEM, INFANT VENTILATOR SYSTEM AND INFANT LS VENTILATOR SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
FLEBOSET DOUBLE
FDA 510(k)
FDA Class 2
·General Hospital
ITREL 3
FDA Adverse Event
Malfunction
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code LGW·June 17, 2013
PULSE GEN MODEL 102R
FDA Adverse Event
Injury
·CYBERONICS, INC.·Product code LYJ·July 20, 2011
PROGRAMMING WAND
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·September 19, 2008
RADIFOCUS GLIDEWIRE ADVANTAGE
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 1, 2020
GLIDEWIRE ADVANTAGE
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 9, 2025
RADIFOCUS GLIDEWIRE ADVANTAGE
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 23, 2022
CAPIOX RX OXYGENATOR
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·March 28, 2019
RADIFOCUS GLIDEWIRE ADVANTAGE
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DQX·February 3, 2025
RADIFOCUS GUIDEWIRE ADVANTAGE
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 12, 2024
RADIFOCUS GLIDEWIRE ADVANTAGE
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code DQX·August 30, 2023
RADIFOCUS GLIDEWIRE ADVANTAGE
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DQX·August 7, 2020