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

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VENTURI NPWT V. II ADVANCED VACUUM SYSTEM

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

N/A

FDA UDI
BIOMET MICROFIXATION, INC·00841036028190·

Millennium

FDA UDI
Avalign Technologies, Inc.·00190776362898·Oral Surgery Exodontia Elevator, #0

SUPPORT SLEEVE

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

HARDYDISK, CIPROFLOXACIN, 5MCG

FDA 510(k)
FDA Class 2 ·Microbiology

CRANE PICK ELEVATOR

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code EMJ·January 15, 2025

CRANE PICK ELEVATOR

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code EMJ·January 14, 2025

ELEVATOR #0

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code EMJ·February 12, 2020

ELEVATOR #0

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code EMJ·January 15, 2025

ELEVATOR #0

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code EMJ·January 15, 2025

ELEVATOR #0

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code EMJ·January 15, 2025

ELEVATOR #0

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code EMJ·November 15, 2019

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·April 17, 2025

INTELLIVUE CLINICAL INFORMATION PORTFOLIO (ICIP)

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code DXJ·April 19, 2013

DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM

FDA Adverse Event
Death ·BAXTER HEALTHCARE CORPORATION·Product code KDI·September 15, 2014

HOMECHOICE LOW RECIRCULATION VOLUME APD SET WITH CASSETTE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·May 16, 2011

ELEVATOR #0

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code EMJ·December 6, 2019

LANX SPINOUS PROCESS FUSION PLATE

FDA Adverse Event
Injury ·LANX, INC.·Product code KWP·March 17, 2011

ELEVATOR #0

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code EMJ·November 4, 2020

BIPAP AUTOSV ADV

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNS·March 10, 2022