12 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HDC SILCATH SUBCLAVIAN CATHETER PERCUTANEOUS INSER
FDA 510(k)
FDA Class 2
·Cardiovascular
Signature
FDA UDI
SILEX MEDICAL, LLC·B3315851078·Allis Grasping Forceps
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704282917·ISRAEL RETRACTOR 9 1/2" 3 PRONGS
Signature
FDA UDI
SILEX MEDICAL, LLC·B331585107845·Long Allis Grasping Forceps
FEATHER-FLEX ADULT ANESTHESIA CIRCUIT
FDA Adverse Event
Malfunction
·BOMIMED INC.·Product code BSJ·August 28, 2014
AutoDensity
FDA 510(k)
FDA Class 2
·Radiology
Arthrex RetroFusion Screw
FDA 510(k)
FDA Class 2
·Orthopedic
MINI-INFUSER RADIATION STERILIZED EXTENSION SETS
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FPA·May 7, 2021
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 5, 2014
FMP HIP
FDA Adverse Event
Other
·ENCORE MEDICAL, L.P.·Product code KWA·November 19, 2012
SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE FOLDABLE INTRAOCULA
FDA Adverse Event
Malfunction
·STAAR SURGICAL CO.·Product code HQL·September 29, 2010
Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.
FDA Enforcement
Class II
·Terminated·STERILMED, INC.·December 16, 2015