8 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BD Single Use, Hypodermic Syringe
FDA 510(k)
FDA Class 2
·General Hospital
Sklar®
FDA UDI
SKLAR CORPORATION·10649111353314·SPENCER WELLS FCP CVD 7"
TOTAL SHOULDER SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MODIFICATION TO: EFLOW ELECTRONIC INHALER/NEBULIZER
FDA 510(k)
FDA Class 2
·Anesthesiology
ZIMMER TRILOGY HIP-LEFT
FDA Adverse Event
Injury
·ZIMMER·Product code LPH·June 12, 2013
PULSE GEN MODEL 102
FDA Adverse Event
Injury
·CYBERONICS, INC.·Product code LYJ·July 20, 2011
COLLEAGUE CX VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 19, 2008
Comprehensive Reverse Shoulder System Humeral Tray Model 115340
FDA Enforcement
Class I
·Terminated·Zimmer Biomet, Inc.·February 22, 2017