11 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ANAX OCT Spinal System
FDA 510(k)
FDA Class 2
·Orthopedic
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100189·MCINTYRE SPECULUM CLOSED WIRE
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100158·KRATZ-BARRAQUER SPECULUM LARGE
HNM Women Care
FDA UDI
HNM STAINLESS, LLC.·00812171028956·PESSARY, OVAL #2, W/O SUPPORT, 2.25"
SunMed
FDA UDI
SUNMED, LLC·20889483000486·CC GUEDEL A/W SZ 70mm BX/50
MILTEX RIGID STERILIZATION CONTAINER SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
CHOICE SPINE VERTEBRAL BODY REPLACEMENT (VBR) DEVICE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Bespa Charcot System
FDA UDI
Kapstone Manufacturing, LLC·00810041320421·Seg Column, Screw, 70
JOSTENT GRAFTMASTER
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MAF·June 6, 2013
IAB : 8 FR - 40 CC FOS
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL INC.·Product code DSP·June 22, 2011
GE OEC 9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 9, 2008