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

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EP-WORKMATE

FDA 510(k)
FDA Class 2 ·Cardiovascular

ADVISOR VITAL SIGNS MONITOR

FDA Adverse Event
Malfunction ·SMITHS MEDICAL PM, INC.·Product code CCK·December 24, 2008

ADVISOR VITAL SIGNS MONITOR

FDA Adverse Event
Malfunction ·SMITHS MEDICAL PM, INC·Product code DQK·April 28, 2010

PILLING

FDA UDI
TELEFLEX INCORPORATED·24026704507645·

LOCATOR F-Tx

FDA UDI
Zest Anchors, LLC·00840481119552·LOCATOR F-Tx Abutment For Large Internal Conica...

LOCATOR R-Tx

FDA UDI
Zest Anchors, LLC·00840481113048·LOCATOR R-Tx Abutment for Large Internal Conica...

THINNER RESOLVE FITNESS MONITOR/BODY SCALE, HEALTH-O-METER

FDA 510(k)
FDA Class 2 ·Cardiovascular

DATEX-OHMEDA AESTIVA/5 WITH 7100 VENTILATOR

FDA 510(k)
FDA Class 2 ·Anesthesiology

FISHER & PAYKEL HEALTHCARE

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·February 11, 2025

FISHER & PAYKEL HEALTHCARE

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·March 3, 2025

FISHER & PAYKEL HEALTHCARE

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·February 23, 2025

FISHER & PAYKEL HEALTHCARE

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·November 27, 2024

880 HUMIDIFICATION SYSTEM

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·March 31, 2010

AISYS

FDA Adverse Event
Malfunction ·DATEX-OHMEDA, INC.·Product code BSZ·January 15, 2016

LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·April 22, 2013

SURESTEP ONE STEP HCG PREGNANCY TEST

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code JHI·April 14, 2011

LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·July 2, 2008

880 HUMIDIFICATION SYSTEM

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LTD.·Product code BTT·February 15, 2010

RESPIRATORY HUMIDIFIER

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·May 12, 2024

RESPIRATORY HUMIDIFIER

FDA Adverse Event
Injury ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·July 4, 2024