60 results · 29ms · Sources: EU EUDAMED, US FDA

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3M MULTIPORE DRY TAPE

FDA Adverse Event
Injury ·3M HEALTH CARE·Product code KGX·March 29, 2017

3M MULTIPORE DRY TAPE

FDA Adverse Event
Injury ·3M HEALTH CARE·Product code KGX·March 29, 2017

3M MULTIPORE DRY TAPE

FDA Adverse Event
Injury ·3M HEALTH CARE·Product code KGX·March 29, 2017

3M MULTIPORE DRY TAPE

FDA Adverse Event
Injury ·3M HEALTH CARE·Product code KGX·March 29, 2017

3M¿ TEGADERM¿ TRANSPARENT FILM DRESSING

FDA Adverse Event
Injury ·3M COMPANY·Product code NAD·September 16, 2025

3M¿ STERI-STRIP¿ REINFORCED ADHESIVE SKIN CLOSURES

FDA Adverse Event
Injury ·3M COMPANY·Product code KGX·September 16, 2025

COBAN 2 LITE LAYER COMPRESSION SYSTEM

FDA Adverse Event
Injury ·3M HEALTH CARE·Product code FQM·December 11, 2017

COBAN 2 LITE LAYER COMPRESSION SYSTEM

FDA Adverse Event
Injury ·3M HEALTH CARE·Product code FQM·December 11, 2017

COBAN 2 LITE LAYER COMPRESSION SYSTEM

FDA Adverse Event
Injury ·3M HEALTH CARE·Product code FQM·December 11, 2017

3M PICC/CVC SECUREMENT DEVICE + TEGADERM CHG CHLORHEXIDINE I. V. SECUREMENT DSG

FDA Adverse Event
Injury ·3M HEALTH CARE·Product code FRO·September 5, 2017

3M PICC/CVC SECUREMENT DEVICE + TEGADERM CHG CHLORHEXIDINE I. V. SECUREMENT DSG

FDA Adverse Event
Injury ·3M HEALTH CARE·Product code FRO·September 5, 2017

3M TEGADERM CHG DRESSING

FDA Adverse Event
Injury ·3M HEALTH CARE·Product code FRO·September 6, 2017

3M¿ MEDIPORE¿ H SOFT CLOTH SURGICAL TAPE

FDA Adverse Event
Injury ·3M COMPANY·Product code KGX·September 16, 2025

2110898-1997-00020

FDA Adverse Event
Injury ·3M COMPANY·Product code FTR·July 15, 1997

2110898-1997-00019

FDA Adverse Event
Injury ·3M COMPANY·Product code FTR·July 15, 1997

2110898-1997-00021

FDA Adverse Event
Injury ·3M SARNS·Product code HRX·July 29, 1997

2110898-1997-00016

FDA Adverse Event
Injury ·Product code HRX·June 11, 1997

2110898-1997-00013

FDA Adverse Event
Injury ·Product code HRX·May 28, 1997

2110898-1996-00005

FDA Adverse Event
Injury ·Product code DRX·October 25, 1996

2110898-1996-00002

FDA Adverse Event
Injury ·Product code HRX·October 1, 1996