86 results · 25ms · Sources: EU EUDAMED, US FDA

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Powder Free White, Blue Sterilized Nitrile Copolymer Surgical Gloves Tested for Use with Chemotherapy Drugs

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

ACTION PRODUCTS, INC.

FDA registration
ACTION PRODUCTS, INC.·8 products·🇺🇸 United States

PTA-DUO PTA BALLOON CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

TRANSPOSAL ULTRA SYSTEMS

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

ARTIS ZEE III CEILING

FDA Adverse Event
Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·May 17, 2024

ARTIS ZEE III CEILING

FDA Adverse Event
Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·December 3, 2024

ARTIS Q ZEEGO

FDA Adverse Event
Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·September 29, 2025

ARTIS ZEE III CEILING

FDA Adverse Event
Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·April 29, 2026

ARTIS ZEE III CEILING

FDA Adverse Event
Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·April 1, 2026

DUO FLUID CART

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·December 21, 2017

ARTIS ZEEGO III (CHINA)

FDA Adverse Event
Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·December 26, 2023

ULTRA DUO HIGH FLUID CART NON-STERILE INSTRUCTIONS FOR USE

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·August 31, 2018

TERUMO CDI 500 BLOOD PARAMETER MONITOR

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·July 1, 2011

TOTAL ASR ACET IMP SIZE 52

FDA Adverse Event
Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·June 20, 2013

TERUMO CENTRIFUGAL SYSTEM

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code KFM·September 29, 2008

ARTIS ZEE III CEILING

FDA Adverse Event
Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·October 28, 2025

ULTRAFLEX DUO HIGH FLUID CART - REFURBISHED

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·June 25, 2020

ARTIS ZEE III FLOOR

FDA Adverse Event
Malfunction ·SIEMENS AG·Product code OWB·September 10, 2024

ARTIS ZEE III FLOOR

FDA Adverse Event
Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·July 12, 2024

ARTIS Q ZEEGO (CHINA)

FDA Adverse Event
Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·May 10, 2024