54 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PASS LP Spinal System
FDA 510(k)
FDA Class 2
·Orthopedic
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741822400·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674182240060·
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X1822400·18mm H x 22mm W x 40mm L x 0 degrees XLIF
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668100974·DESMARRES LID RETRACTOR #2
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X18224080·18mm H x 22mm W x 40mm L x 8 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L182240120·18mm H x 22mm W x 40mm L XLIF Trial 12 degree L...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X182240120·18mm H x 22mm W x 40mm L x 12 degrees XLIF
NIVO NEBULIZER SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
SNTRYPACS
FDA 510(k)
FDA Class 2
·Radiology
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
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