609 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OKI Surgical Planning Software
FDA 510(k)
FDA Class 2
·Radiology
OKI-YOSHITOMA HYDRODISS CAN 27 GA STR
FDA UDI
KATENA PRODUCTS, INC.·00841668140215·OKI-YOSHITOMA HYDRODISS CAN 27 GA STR
OKI-YOSHITOMA HYDRODISS CAN 27 GA 15 DEG
FDA UDI
KATENA PRODUCTS, INC.·00841668140222·OKI-YOSHITOMA HYDRODISS CAN 27 GA 15 DEG
OKI-YOSHITOMI HYDRODISS CAN 23 GA 45 DEG
FDA UDI
KATENA PRODUCTS, INC.·00841668140376·OKI-YOSHITOMI HYDRODISS CAN 23 GA 45 DEG
OKI-YOSHITOMA HYDRODISS CAN 27 GA 30 DEG
FDA UDI
KATENA PRODUCTS, INC.·00841668140239·OKI-YOSHITOMA HYDRODISS CAN 27 GA 30 DEG
OKI-YOSHITOMA HYDRODISS CAN 27 GA 45 DEG
FDA UDI
KATENA PRODUCTS, INC.·00841668140246·OKI-YOSHITOMA HYDRODISS CAN 27 GA 45 DEG
OKI-YOSHITOMI HYDRODISS CAN 23 GA 30 DEG
FDA UDI
KATENA PRODUCTS, INC.·00841668140369·OKI-YOSHITOMI HYDRODISS CAN 23 GA 30 DEG
OKI-YOSHITOMI HYDRODISS CAN 23 GA 25 DEG
FDA UDI
KATENA PRODUCTS, INC.·00841668140352·OKI-YOSHITOMI HYDRODISS CAN 23 GA 25 DEG
ST. JUDE
FDA Adverse Event
Other
·ST. JUDE·Product code DXY·January 8, 2012
AED PLUS
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORP·Product code MKJ·June 6, 2003
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN·Product code CBK·January 24, 2018
8015 ALARIS SYSTEM PC UNIT
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·January 13, 2021
CELL-DYN 1800 ANALYZER
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·December 5, 2012
ESSURE
FDA Adverse Event
Injury
·BAYER MEDICAL CARE INC.·Product code HHS·June 23, 2023
BIRMINGHAM HIP
FDA Adverse Event
Injury
·SMITH AND NEPHEW·Product code NXT·December 27, 2013
SELENIA DIMENSIONS
FDA Adverse Event
Malfunction
·HOLOGIC, INC.·Product code MUE·October 26, 2020
8100 ALARIS PUMP MODULE
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·January 6, 2021
SYMPHONY
FDA Adverse Event
Malfunction
·SORIN CRM·Product code NVZ·October 7, 2016
TENDRIL DX
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL·Product code DTB·August 11, 2023
HAMILTON MEDICAL AG
FDA Adverse Event
Malfunction
·HAMILTON MEDICAL AG·Product code CBK·June 22, 2023