390 results
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33ms
·
Sources: EU EUDAMED, US FDA
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·AED Battery Exchange (Models 9146-ABE, G5-ABE, 5070-ABE, FR3-ABE)
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·DBP-1400-ABE and DBP-2003- ABE
Q-Rejuvalight Pro Facewear
FDA UDI
Light Tree Ventures Europe B.V.·08719327598719·
Q-Rejuvalight Pro Facewear (Model: P19-0023)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
devemed
FDA UDI
devemed GmbH·04061644021284·Filling instrument, spatulate # 4
2.5 / 2.5 mm
...
Tap 5.5
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215039455·
Reicodent
FDA UDI
devemed GmbH·04061644050741·Filling instrument, spatulate # 4
2.5 / 2.5 mm
...
NA
FDA UDI
STRYKER CORPORATION·04546540373106·5.0mm XX-Coarse Diamond Round
NA
FDA UDI
STRYKER CORPORATION·04546540373090·4.0mm XX-Coarse Diamond Round
NA
FDA UDI
STRYKER CORPORATION·04546540373113·6.0mm XX-Coarse Diamond Round
NA
FDA UDI
STRYKER CORPORATION·04546540373120·7.0mm XX-Coarse Diamond Round
WellDoc BlueStar
FDA 510(k)
FDA Class 2
·General Hospital
Reicodent
FDA UDI
devemed GmbH·04061644034925·Filling instrument, spatulate # 4
2.5 / 2.5 mm
...
RESOLUTE INTEGRITY RX
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code NIQ·September 4, 2019
WATCHMAN ® LAA CLOSURE DEVICE & DELIVERY SYSTEM
FDA Adverse Event
Death
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NGV·February 1, 2017
WATCHMAN ® LAA CLOSURE DEVICE & DELIVERY SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NGV·July 1, 2015
RESOLUTE INTEGRITY RX
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code NIQ·January 20, 2018
FLO-GARD 6201 VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FRN·October 8, 2008
8800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 18, 2013
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·August 3, 2011