201 results · 37ms · Sources: EU EUDAMED, US FDA

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CLR MEDICAL, INC.

FDA registration
CLR MEDICAL, INC.·2 products·🇺🇸 United States

CLR Port

FDA UDI
CLR Medical·00860003054918·

CLR Port Injector

FDA UDI
CLR Medical·00850052377007·

CLR Irrigator

FDA UDI
CLR Medical·00860003054901·

CLR Medical

FDA UDI
CLR Medical·00860003054949·

CLR Port Cap

FDA UDI
CLR Medical·00860003054994·

V-LOC 90

FDA Adverse Event
Malfunction ·COVIDIEN LP LLC NORTH HAVEN·Product code GAM·April 4, 2025

V-LOC 90

FDA Adverse Event
Malfunction ·COVIDIEN LP LLC NORTH HAVEN·Product code GAM·April 4, 2025

V-LOC 90

FDA Adverse Event
Malfunction ·COVIDIEN LP LLC NORTH HAVEN·Product code GAM·October 23, 2024

V-LOC 90

FDA Adverse Event
Malfunction ·COVIDIEN LP LLC NORTH HAVEN·Product code GAM·February 13, 2025

V-LOC 90

FDA Adverse Event
Malfunction ·COVIDIEN LP LLC NORTH HAVEN·Product code GAM·January 5, 2023

V-LOC 90

FDA Adverse Event
Malfunction ·COVIDIEN LP LLC NORTH HAVEN·Product code GAM·November 19, 2024

V-LOC 90

FDA Adverse Event
Malfunction ·COVIDIEN LP LLC NORTH HAVEN·Product code GAM·January 24, 2025

V-LOC 90

FDA Adverse Event
Malfunction ·COVIDIEN LP LLC NORTH HAVEN·Product code GAM·January 24, 2025

TUBE RNA PLH 16X100 2.5 PLBLCE CLR

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·April 30, 2020

Viscocel and Viscocel Plus. These products are intraocular fluid devices consisting of non-gaseous fluid intended to be introduced into the eye to aid performance of surgery, such as to maintain anterior chamber depth, preserve tissue integrity, protect tissue from surgical trauma, or function as a tamponade during retinal reattachment.

FDA Recall
Terminated ·C.L.R. Medicals International, Inc.·Product code LZP·November 25, 2013

BD LUER-LOK

FDA Adverse Event
Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·May 8, 2024

BD FACSCALIBUR¿ 4 CLR BASIC SENSOR UNIT

FDA Adverse Event
Malfunction ·BECTON DICKINSON AND COMPANY BD BIOSCIENCES·Product code GKZ·November 2, 2023

MAXPLUS CLR POSITIVE DISPLACEMENT CONN

FDA Adverse Event
Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·January 5, 2021

NV GXL LINR, NTRL, 28MM ID, GROUP 1 CUPS

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JDI·October 11, 2024