68 results · 23ms · Sources: EU EUDAMED, US FDA

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BIOFRIEND BIOMASK SURGICAL FACEMASK, MODELS UNIVERSAL BF-200-2001 AND PREMIUM BF-200-3013

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587P1011280·10mm PLIF Implant 11mm Wide 28mm Length

OrthoMedFlex

FDA UDI
ORTHOMEDFLEX LLC·M7161011280·Kratos Trial Neck, Standard

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587P10112870·10mm PLIF Implant 11mm Wide 28mm Length 7 degrees

Mercodia Iso-Insulin ELISA

FDA UDI
Mercodia AB·07350108630054·Mercodia Iso-Insulin ELISA provides a method fo...

NICHOLS ADVANTAGE DIRECT RENIN (CALIBRATORS, CALIBRATION VERIFIERS, CONTROLS, AND SAMPLE DILUENT)

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

NITRILE EXAM GLOVES, POWDER-FREE, COLOR BLUE

FDA 510(k)
FDA Class 1 ·General Hospital

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICROTYPING SYSTEMS·Product code KSZ·February 23, 2016

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·September 30, 2022

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICROTYPING SYSTEMS·Product code KSZ·November 18, 2015

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICROTYPING SYSTEMS·Product code KSZ·March 8, 2017

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICROTYPING SYSTEMS·Product code KSZ·January 27, 2017

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICROTYPING SYSTEMS·Product code KSZ·August 25, 2016

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICROTYPING SYSTEMS·Product code KSZ·October 6, 2017

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICROTYPING SYSTEMS·Product code KSZ·September 1, 2016

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICROTYPING SYSTEMS·Product code KSZ·September 1, 2016

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICROTYPING SYSTEMS·Product code KSZ·November 25, 2015

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICROTYPING SYSTEMS·Product code KSZ·November 25, 2015

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICROTYPING SYSTEMS·Product code KSZ·June 12, 2015

FORTIFY DR

FDA Adverse Event
Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 9, 2013