8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STERILE AND NON-STERILE O.R. TOWELS, STERILE AND NON-STERILE X-RAY DETECTABLE O.R. TOWELS, SINGLE USE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471121935·K-WIRE - DOUBLE TROCAR 2.0mm DIA x 125mm
DBX STRIP
FDA 510(k)
FDA Class 2
·Orthopedic
Arc EndoCuff and Arc EndoCuff Vision
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SHELL WITH CLUSTER HOLES POROUS 58 MM O.D. SIZE LL
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·February 22, 2019
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·February 14, 2013
RENAL - DISPOSABLE
FDA Adverse Event
Injury
·Product code KDJ·January 17, 2011
AUTOPULSE® RESUSCITATION SYSTEM MODEL 100
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION, INC·Product code DRM·July 28, 2014