53 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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da Vinci Xi Surgical System, da Vinci X Surgical System
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PROPELLER HEAD SCREW SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304269507·
Bernafon
FDA UDI
Bernafon AG·05711584078662·AQ CO9 MNR T, 2.4G NFM DPB MAC/MSIL ACCUQ
PILLING
FDA UDI
TELEFLEX INCORPORATED·24026704513134·
Percutaneous Compression Plate (PC.C.P)
FDA UDI
ORTHOFIX SRL·18032568866087·GOTFRIED PC.C.P. NECK SCREW - 140 MM
n/a
FDA UDI
Hager & Meisinger Gesellschaft mit beschränkter Haftung·E0HM46001822061401·Rotary instrument for endodontic application
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515026797·Doyen Abdominal Retractor, 9 1/2"
Sklar®
FDA UDI
SKLAR CORPORATION·10649111081422·ALLIS TISS FCP DEL 4X5 4"
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668100967·DESMARRES LID RETRACTOR #1
Percutaneous Compression Plate (PC.C.P)
FDA UDI
ORTHOFIX SRL·18033509850585·GOTFRIED PC.C.P. NECK SCREW - 140 MM STERILE
Jett Stem Inserter
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215039592·
XPERT MRSA/SA BLOOD CULTURE ASSAY
FDA 510(k)
FDA Class 2
·Microbiology
FETAL MONITORS, MODELS F2 AND F3
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021