22 results · 33ms · Sources: EU EUDAMED, US FDA

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Stimulator, Stimulator Kit, External Transmitter, External Transmitter Kit

FDA 510(k)
FDA Class 2 ·Neurology

AUFRICHT SABREBACK SCISSORS

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896083899·AUFRICHT SABREBACK SCISSORS STRAIGHT BLADE POWE...

NAFD 100

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

TDK HANDPIECES

FDA 510(k)
FDA Class 1 ·Dental

Widex

FDA UDI
Widex A/S·05706069735772·Widex BEYOND B-F2 (Tan silk S-330 ) Telecoil, R...

BIOGX SARS-COV-2 OSR FOR BD MAX SYSTEM

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO.·Product code QJR·May 22, 2020

U-BLADE SET, TI GAMMA3 10.5X100MM

FDA Adverse Event
Injury ·STRYKER OSETOSYNTHESIS KIEL·Product code HSB·December 18, 2012

GORE TEX VASCULAR GRAFT (TAPERED)

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES, INC·Product code DSY·July 25, 2008

BIFURCATED GORE-TEX STRETCH VASCULAR GRAFT

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES, INC·Product code DSY·August 15, 2008

COLLEAGUE CX VOLUMETRIC INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 20, 2008

ACTIVA RC

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·August 8, 2011

UNKNOWN_OSTEOSYNTHESIS_PRODUCT

FDA Adverse Event
Injury ·STRYKER OSTEOSYNTHESIS-KIEL·Product code HSB·July 2, 2013

PLATE, FIXATION, BONE

FDA Adverse Event
Injury ·DEPUY SYNTHES (USA)·Product code HRS·May 8, 2014

SCREW, FIXATION, BONE

FDA Adverse Event
Malfunction ·DEPUY SYNTHES (USA)·Product code HWC·May 8, 2014

PLATE, FIXATION, BONE

FDA Adverse Event
Malfunction ·DEPUY SYNTHES (USA)·Product code HRS·May 8, 2014

PLATE, FIXATION, BONE

FDA Adverse Event
Injury ·DEPUY SYNTHES (USA)·Product code HRS·May 8, 2014

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·DEPUY SYNTHES (USA)·Product code HWC·May 8, 2014

ONYX

FDA Adverse Event
Malfunction ·COVIDIEN (IRVINE)·Product code MFE·March 29, 2017

ONYX

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3 NEUROVA·Product code MFE·March 29, 2017

ONYX

FDA Adverse Event
Injury ·COVIDIEN (IRVINE)·Product code MFE·March 29, 2017