198 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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UniCel DxH 900 Coulter Cellular Analysis System; UniCel DxH Slidemaker Stainer II Coulter Cellular Analysis System; UniCel DxH 690T Coulter Cellular Analysis System
FDA 510(k)
FDA Class 2
·Hematology
EarQ
FDA UDI
Sbo Hearing A/S·05714464053520·EARQ F20 MINIRITE R C090
Intervertebral Disc Preparation Instruments
FDA UDI
ALPHATEC SPINE, INC.·00190376468587·SLAP HAMMER, HEAVY
16 CH MULTIPURPOSE COIL VARIETY
FDA 510(k)
FDA Class 2
·Radiology
CLEANER ROTATIONAL THROMBECTOMY SYSTEM KIT
FDA 510(k)
FDA Class 2
·Cardiovascular
FLO-GARD 6301 VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FRN·November 24, 2008
ARMADA 14 PTA CATHETER
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code LIT·September 9, 2011
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 22, 2013
UNKNOWN VISION CUP
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MEH·November 29, 2017
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·October 27, 2023
UNKNOWN FEMORAL HEAD
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·November 28, 2017
UNKNOWN FEMORAL HEAD
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·November 28, 2017
UNKNOWN TRILOGY CUP
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·November 29, 2017
UNKNOWN FEMORAL HEAD
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·November 22, 2017
UNKNOWN MULLER CUP
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·November 17, 2017
UNKNOWN TRILOGY CUP
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·November 29, 2017
UNKNOWN HG II CUP
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·November 29, 2017
UNKNOWN BI-METRIC COLLARLESS STEM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDG·November 22, 2017
UNKNOWN BIMETRIC (TITANIUM) STEM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·November 24, 2017
UNKNOWN CUP
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·November 29, 2017