BEUDAMED
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    AD Surgical

    FDA UDI
    APPLIED DENTAL, INC.·00814639023480·Gauze Pads Sterile 3" X 3"

    AD Surgical

    FDA UDI
    APPLIED DENTAL, INC.·00814639023473·Gauze Pads Sterile 2" X 2"

    AD Surgical

    FDA UDI
    APPLIED DENTAL, INC.·00814639023497·Gauze Pads Sterile 4" X 4"

    GZE PCKR&LIG DIR-D/E 2.6mm HF

    FDA UDI
    W.H. Holden, Inc.·D928201161HO0·

    DERMACEA GZE SPG 4X4 12PLY STR

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code NAB·August 30, 2022

    XEROFRM GZE 4X3YD RL FOIL PK STRL

    FDA Adverse Event
    Injury ·COVIDIEN·Product code FRO·October 28, 2016

    XEROFRM GZE 1X8 PTCH FOIL PK STRL

    FDA Adverse Event
    TYCO HEALTHCARE/KENDALL·Product code MGB·August 22, 2003

    61301 STER GZE PADS 100'S 2X2

    FDA Adverse Event
    Injury ·COVIDIEN·Product code NAB·August 3, 2020

    XEROFRM GZE 4X3YD RL FOIL PK STRL

    FDA Adverse Event
    Other ·COVIDIEN·Product code FRO·November 2, 2012

    90102387 DERMACEA GZE SPG 4X4 8PLY STR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code GDY·December 15, 2011

    90102387 DERMACEA GZE SPG 4X4 8PLY STR

    FDA Adverse Event
    Malfunction ·ALLMED MEDICAL PRODUCTS·Product code GDY·January 14, 2016

    AVERY

    FDA Adverse Event
    Injury ·AVERY BIOMEDICAL DEVICES·Product code GZE·April 22, 2009

    DOBELLE INSTITUTE PHRENIC NERVE PACER

    FDA Adverse Event
    Injury ·DOBEL INSTITUTE, INC.·Product code GZE·October 26, 2000

    IMPLANTED DIAPHRAGMATIC/PHRENIC NERVE STIMULATOR

    FDA Adverse Event
    Injury ·AVERY·Product code GZE·August 11, 2023

    *

    FDA Adverse Event
    Injury ·ATROTECHOY·Product code GZE·June 23, 1997

    MEDTRONIC PHRENIC NERVE PAD

    FDA Adverse Event
    Other ·MEDTRONIC USA, INC·Product code GZE·May 15, 2002

    *

    FDA Adverse Event
    Death ·*·Product code GZE·April 13, 1998

    VAS GZE 1X8 CISION DSG FOIL PK STRL

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code GDY·November 16, 2015

    SPNG GZE 4X4IN CRTY 12 PLY PLN LF STRL

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code FRL·May 20, 2026

    Implanted Diaphragmatic/Phrenic Nerve Stimulator

    FDA classification
    FDA Class 3 ·Implanted Diaphragmatic/Phrenic Nerve Stimulator