2,930 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OHL PERIOSTEAL ELEVATOR
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896052758·OHL PERIOSTEAL ELEVATOR DOUBLE ENDED TIPS
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776163310·OHL PERIOSTEAL ELEVATOR DOUBLE ENDED
PERIOSTEAL ELEVATOR OHL #10
FDA UDI
W.H. Holden, Inc.·D9281054360·
Ambler Surgical
FDA UDI
AMBLER SURGICAL CORP.·00190660034337·Ohl periosteal elevator, 7'', double-ended, cur...
1.5T Endorectal Coil
FDA UDI
RAPID Biomedical GmbH·04260487680232·1.5T Endorectal Coil (P-Port)
3.0T Endorectal Coil
FDA UDI
RAPID Biomedical GmbH·04260487680249·3.0T Endorectal Coil
1.5T Endorectal Coil
FDA UDI
RAPID Biomedical GmbH·04260487680416·1.5T Endorectal Coil (A-Port)
UNKNOWN NON-CONTACTING BRIDGING PLATE
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code HRS·November 17, 2022
UNKNOWN NCB PLATE
FDA Adverse Event
Injury
·ZIMMER SWITZERLAND MANUFACTURER GMBH·Product code HRS·November 16, 2022
PAPETTE,500 PER BOX,CYTYC
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code OHL·November 29, 2016
THIN PREP PAP 500 TSTS/CS
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code OHL·April 28, 2016
SUREPATH PRECOAT SLIDE
FDA Adverse Event
Other
·TRIPATH IMAGING, INC.·Product code OHL·March 7, 2008
UNKNOWN NCB PLATE
FDA Adverse Event
Death
·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code HRS·November 18, 2022
UNKNOWN NCB PLATE
FDA Adverse Event
Death
·ZIMMER SWITZERLAND MANUFACTURER GMBH·Product code HRS·November 18, 2022
UNKNOWN NCB PLATE
FDA Adverse Event
Injury
·ZIMMER SWITZERLAND MANUFACTURER GMBH·Product code HRS·November 16, 2022
G4 LONG NAIL LEFT D10XL380MM X 125DEG
FDA Adverse Event
Injury
·STRYKER GMBH·Product code HSB·September 8, 2023
REFORM TI PEDICLE SCREW SYSTEM
FDA Adverse Event
Injury
·PRECISION SPINE, INC·Product code KWP·December 9, 2024
REFORM TI PEDICLE SCREW SYSTEM
FDA Adverse Event
Injury
·PRECISION SPINE, INC·Product code KWP·December 9, 2024
REFORM TI PEDICLE SCREW SYSTEM
FDA Adverse Event
Injury
·PRECISION SPINE, INC·Product code KWP·December 9, 2024
REFORM TI PEDICLE SCREW SYSTEM
FDA Adverse Event
Injury
·PRECISION SPINE, INC·Product code KWP·December 9, 2024