71 results · 24ms · Sources: EU EUDAMED, US FDA

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BACTEC MGIT 960 SIR KITS

FDA 510(k)
FDA Class 2 ·Microbiology

BD BACTEC¿ MGIT¿ 960 SIRE KIT

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·May 6, 2022

BD BACTEC¿ MGIT¿ 960 SIRE KIT

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code MJA·June 30, 2025

BD BACTEC¿ MGIT¿ 960 SIRE KIT

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·September 19, 2023

BD BACTEC¿ MGIT¿ 960 SIRE KIT

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·March 26, 2022

Premier Carvers

FDA UDI
PREMIER DENTAL PRODUCTS COMPANY·00348783009255·Carver DE_C/D Tanner 3T

Oph. Cystotomes

FDA UDI
KATENA PRODUCTS, INC.·00841668113684·CYSTOTOME FORMED 27GA

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523184934·Kerrison Rongeur, Angled Left - 5mm

CORDIS TRAPEASE PERMANENT VENA CAVA FILTER AND INTRODUCTION KIT

FDA 510(k)
FDA Class 2 ·Cardiovascular

MODIFICATION TO ZEUS SCIENTIFIC, INC., TPO IGG ELISA TEST SYSTEM

FDA 510(k)
FDA Class 2 ·Immunology

MultiPolar®

FDA UDI
Zimmer, Inc.·00889024116276·

MECHANICAL (MANUAL) WHEELCHAIR

FDA Adverse Event
Malfunction ·INVAMEX·Product code IOR·March 13, 2013

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·February 8, 2011

SM204 M-SERIES W/BIG WHEEL

FDA Adverse Event
Other ·STRYKER CORP., MEDICAL DIVISION·Product code FPO·February 22, 2008

Zenlens Toric-Gas Permeable Contact lenses for Daily Wear in a 10-cc polycarbonate vial (Rx) as follows: Zenlens FT(Front Toric); Zenlens Toric-Zenlens FT + MV (Front Toric+Microvault); Zenlens TPC-(Toric Peripheral Curve); Zenlens TPC + FT- (Toric Peripheral Curve + FrontToric) Zenlens TPC + MV- (Toric Peripheral Curve+Microvault). Catalog Number: AOZNT Zenlens Toric - Zenlens contact lenses are indicated for daily wear for the correction of refractive arnetropia (myopia, hyperopia, and astigmatism) in aphakic and nonaphakic persons with non-diseased eyes.

FDA Enforcement
Class III ·Terminated·Alden Optical·September 12, 2018

V500, SAVINA AND VENTILATORS OF EVITA FAMILY

FDA Adverse Event
Other ·DRAGER MEDICAL GMBH·Product code CBK·February 18, 2011

ACTIVELIFE

FDA Adverse Event
Malfunction ·CONVATEC DOMINICAN REPUBLIC INC·Product code EZQ·November 13, 2018

ACTIVELIFE

FDA Adverse Event
Malfunction ·CONVATEC DOMINICAN REPUBLIC INC·Product code EZQ·November 13, 2018

ACTIVELIFE

FDA Adverse Event
Malfunction ·CONVATEC DOMINICAN REPUBLIC INC·Product code EZQ·November 13, 2018

ACTIVELIFE

FDA Adverse Event
Malfunction ·CONVATEC DOMINICAN REPUBLIC INC·Product code EZQ·November 13, 2018