22 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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SPINEFRONTIER LUMBAR IBF SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
A Series
FDA UDI
Respironics, Inc.·00606959041028·A Series System One Heated Humidifier, Japan
Surgical Instrument
FDA UDI
Jeil Medical Corporation·08800089456109·
MicroSelectron Digital
FDA UDI
Nucletron B.V.·08717213033849·Coupling Treatment Tube for 5F Flexibles (21)
Summa Orthopaedics System Surgical Instrument
FDA UDI
Jeil Medical Corporation·08800089466696·
ASAHI TREASURE FLOPPY PERIPHERAL GUIDE WIRE
FDA 510(k)
FDA Class 2
·Cardiovascular
SENTRYSUITE PRODUCT LINE
FDA 510(k)
FDA Class 2
·Anesthesiology
LONG NAIL KIT R2.0, TI, RIGHT GAMMA3 Ø11X380MM X 125°
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS-KIEL·Product code HSB·April 12, 2013
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523108442·Polyaxial Screw 5.5mm diameter 40mm length for ...
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523108428·Polyaxial Screw 5.5mm diameter 30mm length for ...
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523108480·Polyaxial Screw 5.5mm diameter 60mm length for ...
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523108459·Polyaxial Screw 5.5mm diameter 45mm length for ...
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523108411·Polyaxial Screw 5.5mm diameter 25mm length for ...
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523108473·Polyaxial Screw 5.5mm diameter 55mm length for ...
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523108435·Polyaxial Screw 5.5mm diameter 35mm length for ...
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523108466·Polyaxial Screw 5.5mm diameter 50mm length for ...
NEU_INTERSTIM_INS
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code EZW·August 28, 2012
DEPUY ASR XL FEM IMP SIZE 47
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·May 14, 2013
ARTICULEZE M HEAD 36MM -2
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·May 13, 2011
BIOFLEX TESIO
FDA Adverse Event
Injury
·MEDCOMP·Product code MSD·August 13, 2008