32 results · 26ms · Sources: EU EUDAMED, US FDA

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Zio Monitor

FDA 510(k)
FDA Class 2 ·Cardiovascular

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112946·CORNEAL TREPHINE BLADE8.25MM

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112526·BARRON VACUUM TREPHINE 8.25MM

MDI GLIADIN G TEST

FDA 510(k)
FDA Class 2 ·Immunology

PICASSO/ PICASSO LITE/ PICASSO PERIO

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

LIFEPAK CR(R) PLUS DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·November 4, 2013

LIFEPAK CR(R) PLUS DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·March 3, 2014

RESOLUTION CLIP DEVICE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MND·October 16, 2008

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 11, 2011

SYNCHROMED II

FDA Adverse Event
Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 2, 2013

LIFEPAK CR(R) PLUS DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·August 28, 2013

MICRA

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code PNJ·February 13, 2023

NI

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code DYE·June 20, 2024

NI

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code DYE·June 20, 2024

NI

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code DYE·June 20, 2024

ONYX

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·July 7, 2023

NI

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code DYE·June 20, 2024

GORE® VIABAHN® ENDOPROSTHESIS WITH HEPARIN BIOACTIVE SURFACE

FDA Adverse Event
Injury ·W. L. GORE & ASSOCIATES, INC.·Product code NIP·May 24, 2024

NI

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code DYE·June 20, 2024

NI

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code DYE·June 20, 2024