23 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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EZSENSOR P DIGITAL INTRAORAL SENSOR
FDA 510(k)
FDA Class 2
·Radiology
Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780377139·Integra® Jarit® Crile-Wood Needle Holder, 8", C...
CHS
FDA UDI
Smith & Nephew, Inc.·03596010062055·AMBI COMPRESSION HIP SCREW PLATE 4SL 100MM 140D
MOBIS XL 0°
FDA UDI
SIGNUS Medizintechnik GmbH·04047844001714·The KIMBA®, KIMBA® mini, MOBIS® and NOVAL™ impl...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587P1211320·12mm PLIF Implant 11mm Wide 32mm Length
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587P12113270·12mm PLIF Implant 11mm Wide 32mm Length 7 Degrees
TM "Soloventex" 121-132 XL
FDA UDI
REABILITIMED TOV·04823097718407·Women's closed-toe socks, 2nd compression class...
TM "Soloventex" 121-132 S
FDA UDI
REABILITIMED TOV·04823097718377·Women's closed-toe socks, 2nd compression class...
TM "Soloventex" 121-132 M
FDA UDI
REABILITIMED TOV·04823097718384·Women's closed-toe socks, 2nd compression class...
TM "Soloventex" 121-132 XXL
FDA UDI
REABILITIMED TOV·04823097718414·Women's closed-toe socks, 2nd compression class...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197380973·Super-Cut Gradle Walton Scissors
straig...
TM "Soloventex" 121-132 L
FDA UDI
REABILITIMED TOV·04823097718391·Women's closed-toe socks, 2nd compression class...
UNI-PATCH ULTRASOUND COUPLING GEL
FDA 510(k)
FDA Class 2
·Radiology
POWDER FREE VINYL PATIENT EXAMINATION GLOVES, (BLUE, WHITE, PINK)
FDA 510(k)
FDA Class 1
·General Hospital
CARB-BITE CRILE-WOOD NH 8
FDA Adverse Event
Malfunction
·INTEGRA LIFESCIENCES MANSFIELD·Product code DWS·August 5, 2022
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·May 20, 2013
TANDEM T:SLIM INSULIN DELIVERY SYSTEM
FDA Adverse Event
Injury
·TANDEM DIABETES CARE, INC.·Product code LZG·September 24, 2014
RF MULTIGEN
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS KALAMAZOO·Product code GXD·May 4, 2011
TRUE METRIX AIR
FDA Adverse Event
Malfunction
·TRIVIDIA HEALTH INC·Product code NBW·April 25, 2024
HEARTWARE VENTRICULAR ASSIST SYSTEM- PUMP
FDA Adverse Event
Injury
·HEARTWARE, INC.·Product code DSQ·February 14, 2019