27 results · 22ms · Sources: EU EUDAMED, US FDA

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Stryker Facial iD System

FDA 510(k)
FDA Class 2 ·Dental

Ophthalmic Spatula

FDA UDI
KATENA PRODUCTS, INC.·00841668102534·KNOLLE LENS NUCLEUS SPATULA

SR-1000 Portable DR Imaging System, SR-1000S Portable DR Imaging System

FDA 510(k)
FDA Class 2 ·Radiology

INFRARED SCIENCES BREASTSCAN IR SYSTEM

FDA 510(k)
FDA Class 1 ·Obstetrics/Gynecology

CADD

FDA Adverse Event
Malfunction ·ST PAUL·Product code FPA·June 1, 2022

CADD

FDA Adverse Event
Malfunction ·ST PAUL·Product code FPA·June 1, 2022

CADD

FDA Adverse Event
Malfunction ·ST PAUL·Product code FPA·June 1, 2022

CADD

FDA Adverse Event
Malfunction ·ST PAUL·Product code FPA·June 1, 2022

PORTEX BLUE LINE ULTRA CUFFED TRACHEOSTOMY TUBE

FDA Adverse Event
Malfunction ·SMITHS MEDICAL INTERNATIONAL LTD.·Product code BTO·October 23, 2014

PINNACLE MTL INS NEUT36IDX52OD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·August 18, 2011

TEN20 CONDUCTIVE PASTE

FDA Adverse Event
Injury ·D.O. WEAVER CO.·Product code GYB·December 10, 2012

CADD ADMINISTRATION SETS - FLOW STOP

FDA Adverse Event
Malfunction ·ST PAUL·Product code FPA·May 23, 2022

VGXP XP E1 TIB BRG RM 10X71

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code MBH·May 29, 2015

VGXP XP E1 TIB BRG RL 10X71

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code MBH·May 29, 2015

VANGUARD ANTERIOR STABILIZED TIBIAL BEARING

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·July 16, 2019

VANGUARD CRUCIATE RETAINING FEMORAL

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·July 15, 2019

VANGUARD AS TIBIAL BEARING

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·July 19, 2019

BIOMET CC CRUCIATE TRAY

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code MBH·July 15, 2019

BIOMET MODULAR TIBIAL LOCKING BAR

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·July 22, 2019

VANGUARD CR FEMORAL

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·July 19, 2019