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

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EXHALATION VALVE

FDA 510(k)
FDA Class 2 ·Anesthesiology

NexxZr™ T / D-100-35-NT-C400-SD

FDA UDI
SAGEMAX BIOCERAMICS, INC·00842271113535·

LIQUID OXYGEN SYSTEM

FDA 510(k)
FDA Class 2 ·Anesthesiology

SUSPENSION ACROMIOCLAVICULAR (AC) REPAIR SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

UV PHOTOTHERAPY

FDA Adverse Event
Injury ·UNK·Product code FTC·January 27, 2021

UV PHOTOTHERAPY

FDA Adverse Event
Injury ·XUZHOU KERNEL MEDICAL INSTRUMENT EQUIPMENT CO.·Product code FTC·November 30, 2022

WAVEWRITER ALPHA?

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·March 24, 2026

UV PHOTOTHERAPY

FDA Adverse Event
Injury ·UNK·Product code FTC·January 25, 2021

UV PHOTOTHERAPY LAMP

FDA Adverse Event
Injury ·ANGEL KISS LLC.·Product code FTC·February 3, 2021

UV PHOTOTHERAPY

FDA Adverse Event
Injury ·UNK·Product code FTC·January 26, 2021

UV PHOTOTHERAPY LAMP

FDA Adverse Event
Injury ·UNK·Product code FTC·January 29, 2021

UV PHOTOTHERAPY

FDA Adverse Event
Injury ·ANGEL KISS LLC·Product code FTC·February 2, 2021

UV PHOTOTHERAPY LAMP

FDA Adverse Event
Injury ·ANGEL KISS LLC.·Product code FTC·February 4, 2021

MAXZERO NEEDLELESS CONNECTOR

FDA Adverse Event
Malfunction ·CAREFUSION·Product code FPA·January 6, 2020

ETRIO

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·May 29, 2013

560 BIO-CONSOLE BASE UNIT

FDA Adverse Event
Injury ·MEDTRONIC PERFUSION SYSTEMS·Product code DWA·June 10, 2011

GORE EXCLUDER AAA ENDOPROSTHESIS

FDA Adverse Event
Injury ·W. L. GORE & ASSOCIATES·Product code MIH·August 22, 2008

MAXZERO NEEDLELESS CONNECTOR

FDA Adverse Event
Malfunction ·CAREFUSION·Product code FPA·September 2, 2020

MAXZERO NEEDLELESS CONNECTOR

FDA Adverse Event
Malfunction ·CAREFUSION·Product code FPA·May 8, 2020

MAXZERO NEEDLELESS CONNECTOR

FDA Adverse Event
Malfunction ·CAREFUSION·Product code FPA·May 8, 2020