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

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MUTARS® femoral stem cemented 160 mm and 200 mm

FDA 510(k)
FDA Class 2 ·Orthopedic

ProCare Nebulizer Basic

FDA UDI
ARISE MEDICAL LLC·00372217005018·ProCare Nebulizer Basic

Delta®

FDA UDI
MEDTRONIC PS MEDICAL, INC.·00643169497597·SHUNT 24039-1 DELTA REG PL 1.0 90CM

MPACT Extension

FDA 510(k)
FDA Class 2 ·Orthopedic

TOTAL BILIRUBIN REAGENT SET

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

MPACT ACETABULAR SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·October 31, 2025

MPACT EXTENSION

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·April 2, 2026

MPACT ACETABULAR SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·July 18, 2025

MECTACER BIOLOX DELTA FEMORAL BALL HEAD

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·December 19, 2024

AMISTEM-P

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·August 26, 2025

MECTACER BIOLOX DELTA FEMORAL BALL HEAD

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·November 18, 2025

MPACT ACETABULAR SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·December 19, 2025

MPACT ACETABULAR SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·November 21, 2024

AMISTEM-P COLLARED

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·January 13, 2025

LINER: MPACT FLAT PE HC LINER Ø28/B

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·August 3, 2022

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·November 10, 2014

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN INC.·Product code NBW·September 9, 2011

DUROM US ACETABULAR COMPONENT 58/52 R

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·July 18, 2013

ALARIS SYSTEM

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·October 27, 2023

BD MINIDRAW¿ FINGER SLEEVE, EXTRA-LARGE

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·March 5, 2025