20 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Coconut Infused Hybrid Personal Lubricant
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Lateral Patient Positioning System
FDA UDI
ALPHATEC SPINE, INC.·00190376474717·Strap, Single Closure, 42"
N/A
FDA UDI
Ortho Development Corporation·00822409129591·Uni Distal Cut Guide Size +2 Left
Lateral Patient Positioning System
FDA UDI
ALPHATEC SPINE, INC.·00190376474694·Strap, Single Closure, 30"
Lateral Patient Positioning System
FDA UDI
ALPHATEC SPINE, INC.·00190376474663·Strap, Single Closure, 66"
Lateral Patient Positioning System
FDA UDI
ALPHATEC SPINE, INC.·00190376474724·Strap, Single Closure, 48"
Lateral Patient Positioning System
FDA UDI
ALPHATEC SPINE, INC.·00190376475592·Strap, Single Closure, 96"
Lateral Patient Positioning System
FDA UDI
ALPHATEC SPINE, INC.·00190376475561·Strap, Single Closure, 78"
Lateral Patient Positioning System
FDA UDI
ALPHATEC SPINE, INC.·00190376474687·Strap, Single Closure, 76"
Lateral Patient Positioning System
FDA UDI
ALPHATEC SPINE, INC.·00190376475578·Strap, Single Closure, 84"
Lateral Patient Positioning System
FDA UDI
ALPHATEC SPINE, INC.·00190376474670·Strap, Single Closure, 72"
Lateral Patient Positioning System
FDA UDI
ALPHATEC SPINE, INC.·00190376475585·Strap, Single Closure, 90"
Lateral Patient Positioning System
FDA UDI
ALPHATEC SPINE, INC.·00190376474700·Strap, Single Closure, 36"
Lateral Patient Positioning System
FDA UDI
ALPHATEC SPINE, INC.·00190376474731·Strap, Single Closure, 54"
Lateral Patient Positioning System
FDA UDI
ALPHATEC SPINE, INC.·00190376474748·Strap, Single Closure, 60"
RESOUND ENDOSCOPIC ULTRASOUND ASPIRATION NEEDLE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SERIM HISENSE ULTRA 0.1, PART NUMBER 5167
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ULTRA 360 PATIENT POSITIONING SYSTEM
FDA Adverse Event
Malfunction
·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code FWZ·October 15, 2014
DIMENSION VISTA CLINICAL CHEMISTRY SYSTEM
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·June 20, 2013
RESTORE ULTRA
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·July 7, 2011