15 results · 21ms · Sources: EU EUDAMED, US FDA

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NIPRO HYPODERMIC NEEDLE

FDA 510(k)
FDA Class 2 ·General Hospital

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·24026704284348·ADSON RETRACTOR 12 1/2" 4 X 5 BLUNT

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·14026704920836·

3.0T 4-CHANNEL CERVICO-THORACIC-LUMBAR (CTL) ARRAY COIL

FDA 510(k)
FDA Class 2 ·Radiology

ATAC PAK CPK REAGENT KIT

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

9611993-2022-052474

FDA Adverse Event
Injury ·NOBEL BIOCARE (PRODUCTION) AB·Product code DZE·April 4, 2022

BOM 7MM EXTENDED LENGTH ENDOSCOPE

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR LLC·Product code GCJ·March 27, 2019

CONTOUR THREAD OR CONTOUR THREADS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES (DBA ANGIOTECH)·Product code GAW·April 3, 2008

VASO VIEW HEMOPRO

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR LLC·Product code GEI·April 8, 2019

VASOVIEW HEMOPRO 2

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR LLC·Product code GEI·April 13, 2019

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Injury ·ANIMAS CORPORATION·Product code LZG·April 11, 2013

PHILOS II DR

FDA Adverse Event
Malfunction ·BIOTRONIK SE & CO. KG·Product code NVZ·March 15, 2011

TERUMO ADVANCED PERFUSION SYSTEM

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code KFM·May 22, 2008

VASO VIEW HEMOPRO

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR LLC·Product code GEI·April 15, 2019

Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone

FDA Enforcement
Class II ·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012