27 results
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38ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BLUE SKY BIO DENTAL IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
CREA Reagent Kit
FDA UDI
MEDICA CORPORATION·00386100001995·Creatinine Reagent Kit for use with EasyRA Anal...
PINNACLE
FDA UDI
TERUMO MEDICAL CORPORATION·00389701008561·PINNACLE TIF Introducer Sheath
SPIRA-A
FDA UDI
CAMBER SPINE TECHNOLOGIES, LLC·B030SPA1020340·Trial, 30 x 38mm, 15° Lordotic, 17mm
SPIRA-L
FDA UDI
CAMBER SPINE TECHNOLOGIES, LLC·B030SPL1020340·Trial, Bi-Convex, 15° Lordotic, 18 x 60mm, 14mm
SPIRA-O
FDA UDI
CAMBER SPINE TECHNOLOGIES, LLC·B030SPO1020340·Trial Bi-Convex 20° Lordotic, 30mm x 33mm, 15mm
Ti-Diagon
FDA UDI
CAMBER SPINE TECHNOLOGIES, LLC·B030DIT1020340·TLIF Trial, 26 x 11mm, 15° Lordotic, 15mm
SPIRA-C
FDA UDI
CAMBER SPINE TECHNOLOGIES, LLC·B030SPC1020340·Trial,12mm x 14.5mm Lordotic 7°, 6mm
SPIRA®-A Integrated
FDA UDI
CAMBER SPINE TECHNOLOGIES, LLC·B030SAZ1020340·SPIRA®-A Integrated,Trial, 26x34mm, 15° Lordoti...
HM-LAMP II
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MODIFICATION TO: SIPAP INFANT NASAL CPAP CIRCUIT
FDA 510(k)
FDA Class 2
·Anesthesiology
UniTip Catheter
FDA UDI
Unisensor AG·07640172971956·
V200 / ESPRIT
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code CBK·March 16, 2021
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code CBK·March 28, 2021
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code MNT·May 19, 2021
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code CBK·May 20, 2021
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code MNT·June 7, 2021
V200 VENTILATOR
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, INC·Product code CBK·December 9, 2020
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code MNT·June 21, 2021
OCTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 6, 2013