40 results · 31ms · Sources: EU EUDAMED, US FDA

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MICROSCAN SYNERGIES PLUS GRAM POSITIVE MIC/COMBO PANELS NEW ANTIMICROBIAL-STREPTOMYCIN SYNERGY SCREEN

FDA 510(k)
FDA Class 2 ·Microbiology

DP-REPAIR

FDA UDI
Denplus Inc·D8451071316·DP-REPAIR-F, ORI, 11.3 kg

PMMA disc

FDA UDI
Dentsply International Inc.·D00180713160·

APEX Knee System

FDA UDI
Omni Life Science, Inc.·00841690191728·Revision Tibia Impactor Pad (Green)

INTREX

FDA UDI
Conmed Corporation·10845854009505·INTREX LARGE BONE OSCILLATING SAW BLADE 25.0 X ...

BIOCURVE SOFT (HIOXIFILCOM A) SPHERICAL AND TORIC SOFT CONTACT LENS FOR DAILY WEAR (CLEAR AND BLUE VISIBILITY-HANDLING T

FDA 510(k)
FDA Class 2 ·Ophthalmic

ULTRA N-GENEOUS HDL CHOLESTEROL REAGENT 1/REAGENT2; ULTRA N-GENEOUS HDL CHOLESTREOL CALIBRATOR

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

LINEAR ST

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 17, 2020

S5 ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 26, 2012

S5 ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012

S5 ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012

S5 SYSTEM

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

S5 ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 6, 2012

S5 ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 6, 2012

S5 SYSTEM

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

S5 SYSTEM

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

S5 SYSTEM

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

S5 SENSOR MODULE FOR BUBBLE DETECTOR

FDA Adverse Event
Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTW·October 21, 2016

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·April 22, 2013

FLAIR ENDOVASCULAR STENT GRAFT

FDA Adverse Event
BARD PERIPHERAL VASCULAR, INC.·Product code MIH·April 18, 2011