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AVID MEDICAL, INC. A MEDICAL ACTION IND. COMPANY 305

FDA registration
AVID MEDICAL, INC. A MEDICAL ACTION IND. COMPANY 305·77 products·🇺🇸 United States

UNK

FDA Adverse Event
AVID MEDICAL, INC.·Product code MED·February 20, 2015

AVID MEDICAL, INC

FDA Adverse Event
Injury ·AVID MEDICAL, INC.·Product code LRO·July 3, 2001

AVID MEDICAL INC.

FDA Adverse Event
AVID MEDICAL INC.·Product code KDD·November 25, 2015

ICU MEDICAL INC.

FDA Adverse Event
Malfunction ·ICU MEDICAL INC.·Product code DRS·August 24, 2017

ICU MEDICAL INC.

FDA Adverse Event
Malfunction ·ICU MEDICAL INC.·Product code DRS·August 24, 2017

HALYARD

FDA Adverse Event
Malfunction ·LA ADA DE ACUNA, S. DE. R. L. DE C. V.·Product code PUI·May 21, 2019

HALYARD

FDA Adverse Event
Malfunction ·LA ADA DE ACUNA, S. DE. R. L. DE C. V.·Product code PUI·July 5, 2019

HALYARD

FDA Adverse Event
Malfunction ·LA ADA DE ACUNA, S. DE. R. L. DE C. V.·Product code PUI·July 5, 2019

AVID MEDICAL

FDA Adverse Event
Injury ·AVID MEDICAL, INC. A MEDICAL ACTION IND. COMPANY·Product code LRO·December 17, 2019

AVID MEDICAL

FDA Adverse Event
Injury ·AVID MEDICAL, INC. A MEDICAL ACTION IND. COMPANY·Product code LRO·December 17, 2019

AVID MEDICAL

FDA Adverse Event
Injury ·AVID MEDICAL, INC. A MEDICAL ACTION IND. COMPANY·Product code LRO·December 17, 2019

AVID MEDICAL

FDA Adverse Event
Injury ·AVID MEDICAL, INC. A MEDICAL ACTION IND. COMPANY·Product code LRO·December 17, 2019

AVID MEDICAL

FDA Adverse Event
Injury ·AVID MEDICAL, INC. A MEDICAL ACTION IND. COMPANY·Product code LRO·December 17, 2019

1047429-2015-00003

FDA Adverse Event
October 15, 2015

A PLUS INTERNATIONAL INC.

FDA Adverse Event
Injury ·A PLUS INTERNATIONAL INC·Product code GDY·May 1, 2019

ACCU-LINE

FDA Adverse Event
Injury ·ACCU-LINE PRODUCTS INC.·Product code FZZ·May 9, 2019

RICHARD-ALLAN / ASPEN SURGICAL PRODUCTS

FDA Adverse Event
ASPEN SURGICAL PRODUCTS, INC.·Product code GAB·December 15, 2016

US MEDCO INC

FDA Adverse Event
Malfunction ·US MEDCO, INC.·Product code GDY·June 1, 2018

GAUZE 8X4 DUAL XRAY 10'S

FDA Adverse Event
Malfunction ·WELMED INC.·Product code GDY·January 25, 2010