14 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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One Mum Pumpset
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
MOUNT-2A
FDA UDI
Aktormed GmbH·04260463840674·
External Fixation
FDA UDI
Life Spine, Inc.·00190837034009·Wire Tensioner
N95 SURGICAL RESPIRATOR, TYPE AP0018 AND AP0028
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ENDOSKELETON TO
FDA 510(k)
FDA Class 2
·Orthopedic
RIVA STAR SILVER DIAMINE FLUORIDE
FDA Adverse Event
Injury
·SDI LIMITED·Product code LBH·February 13, 2019
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 22, 2011
PLUM XLD 110V L.A.
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·June 11, 2013
TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·September 23, 2008
FILIFORM DOUBLE PIGTAIL URETERAL STENT SET
FDA Adverse Event
Malfunction
·COOK INC·Product code FAD·June 30, 2022
FILIFORM DOUBLE PIGTAIL URETERAL STENT SET
FDA Adverse Event
Malfunction
·COOK INC·Product code FAD·June 30, 2022
INVISION¿ TOTAL ANKLE SYSTEM
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY INC·Product code HSN·July 18, 2022
BLACK SILICONE FILIFORM DOUBLE PIGTAIL URETERAL STENT
FDA Adverse Event
Malfunction
·COOK INC·Product code FAD·January 31, 2023
FILIFORM DOUBLE PIGTAIL URETERAL STENT SET
FDA Adverse Event
Malfunction
·COOK INC·Product code FAD·January 2, 2020