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

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Encompass SRS Headframe ; Encompass MR SRS Headframe

FDA 510(k)
FDA Class 2 ·Radiology

Bernafon

FDA UDI
Bernafon AG·05711584076040·CAPTO 7 FW 1.0

THERMO PAL INFRARED EAR THERMOMETER

FDA 510(k)
FDA Class 2 ·General Hospital

POWDER FREE NITRLE EXAMINATION GLOVES WITH CHEMOTHERAPY LABELING CLAIM

FDA 510(k)
FDA Class 1 ·General Hospital

PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·March 31, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 30, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 20, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 8, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·March 20, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·March 19, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 23, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 29, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 24, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 27, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 22, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 15, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·March 19, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 16, 2026

BD PLASTIPAK LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 15, 2026

UNICEL® DXI 800 ACCESS® IMMUNOASSAY SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER INC.·Product code JJE·May 12, 2011