27 results
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29ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SOFIA ANALYZER AND INFLUENZA A+B FIA
FDA 510(k)
FDA Class 2
·Microbiology
9301 HAND CONTROLLER
FDA UDI
HANS RUDOLPH, INC.·00874750008131·PNEU HAND CNTRL SWITCH 9301
Surgical Instrument
FDA UDI
Jeil Medical Corporation·08800089476312·
Surgical Instrument
FDA UDI
Jeil Medical Corporation·08800089476275·
Surgical Instrument
FDA UDI
Jeil Medical Corporation·08800089476305·
Surgical Instrument
FDA UDI
Jeil Medical Corporation·08800089476268·
Surgical Instrument
FDA UDI
Jeil Medical Corporation·08800089476282·
Surgical Instrument
FDA UDI
Jeil Medical Corporation·08800089476299·
SENSICARE POWDER-FREE POLYMER COATED POLYSOPRENE SURGICAL GLOVES, STERILE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
VENTVIEW, MODEL 8414095
FDA 510(k)
FDA Class 2
·Anesthesiology
SURESTEP
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·October 16, 2003
CASPIAN Spinal System
FDA UDI
VB Spine LLC·10888857242456·Occipital Plate, Tap Size Ø5.25 mm
CASPIAN Spinal System
FDA UDI
VB Spine LLC·10888857242449·Occipital Plate, Tap Size Ø4.5 mm
BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAVED KIT
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·April 12, 2024
BIPAP PRO BIFLEX
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·December 1, 2025
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·September 23, 2014
D-TRONPLUS POWER PACK
FDA Adverse Event
Malfunction
·DISETRONIC MEDICAL SYSTEMS, INC.·Product code LZG·July 16, 2007
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·June 3, 2011
BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAVED KIT
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·April 24, 2024
BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAVED KIT
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL DEVICES CO., LTD. SUZHOU·Product code PSZ·January 22, 2024