20 results · 30ms · Sources: EU EUDAMED, US FDA

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GUINEA PIG WHOLE SERUM

FDA 510(k)
FDA Class 1 ·Hematology

Triad

FDA UDI
Nuvasive, Inc.·00887517265029·Triad Cervical Rasp, 9x11x11mm

Washbon

FDA UDI
ORMCO CORPORATION·00889989043709·UPPER LEFT FIRST MOLAR WASHBON BAND SIZE 9

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·BYREL PROGRAMABLE PACEMAKER

NOVABONE PUTTY- BIOACTIVE SYNTHETIC GRAFT

FDA 510(k)
FDA Class 2 ·Orthopedic

COLORIMETRIC DETERMINATION (LDH)

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·BYREL PROGRAMABLE PACEMAKER

ALARIS® PUMP MODULE ADMINISTRATION SET

FDA Adverse Event
Malfunction ·CAREFUSION·Product code FPA·January 12, 2017

ALARIS® PUMP MODULE ADMINISTRATION SET

FDA Adverse Event
Malfunction ·CAREFUSION·Product code FPA·May 10, 2018

ALARIS PUMP MODULE ADMINISTRATION SET

FDA Adverse Event
Malfunction ·CAREFUSION·Product code FPA·November 13, 2017

FLEXTEND

FDA Adverse Event
Malfunction ·CPI - DEL CARIBE·Product code NVN·October 10, 2012

SPECTRUM INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·December 3, 2013

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN, INC.·Product code NBW·August 2, 2010

ALARIS SECONDARY SET

FDA Adverse Event
Malfunction ·CAREFUSION·Product code FPA·November 14, 2016

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·May 10, 2013

Peri GYN, Kit number PSS2193(A convenience custom kits used for general surgery in hospital operating room

FDA Enforcement
Class II ·Terminated·Windstone Medical Packaging, Inc.·October 26, 2016

ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION·Product code FRN·February 25, 2019

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·August 4, 2014

INFUSION ADAPTER C100-O

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code ONB·September 9, 2024

ALARIS PUMP MODULE

FDA Adverse Event
Injury ·CAREFUSION·Product code FRN·March 31, 2017