14 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TRANSCRANIAL DOPPLER WITH ROBOTIC PROBE HEADBAND
FDA 510(k)
FDA Class 2
·Radiology
HEX-FIX
FDA UDI
Smith & Nephew, Inc.·03596010069443·TITANIUM HALF PIN 5.0MM X 35MM
ArgenZ HT+ 95x14 D4
FDA UDI
ARGEN CORPORATION, THE·D818122710·Dental porcelain/ceramic restoration kit
BECHERT LENS NUCLEUS ROTATOR
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896013360·BECHERTLENS NUCLEUS ROTATOR ANGLED BLUNT FORKED...
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K1220100·Breaker, Extended Tab
Plateau V & Z
FDA UDI
Life Spine, Inc.·00190837073237·Plateau V Spacer, 11mm x 22mm x 10mm,7 degree
BECHERT LENS NUCLEUS ROTATOR
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896013322·BECHERT LENS NUCLEUS ROTATOR ANGLED BLUNT FORKE...
SMARTPACS
FDA 510(k)
FDA Class 2
·Radiology
NEO-SERVO I
FDA 510(k)
FDA Class 2
·General Hospital
GORE® VIABAHN® ENDOPROSTHESIS WITH HEPARIN BIOACTIVE SURFACE
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code NIP·September 9, 2021
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2013
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code IOR·September 26, 2014
ASR UNI FEMORAL IMPL SIZE 46
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 3, 2011
UNKNOWN IMPLANT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWY·May 15, 2023