22 results · 21ms · Sources: EU EUDAMED, 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