2,079 results
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62ms
·
Sources: EU EUDAMED, US FDA
REACH MEDICAL, INC.
FDA registration
REACH MEDICAL, INC.·1 product·🇺🇸 United States
EDP
FDA UDI
REACH MEDICAL, INC.·00850004857069·External Penile Rigidity Device Manual and Batt...
EDP MAXRC
FDA UDI
REACH MEDICAL, INC.·00850004857106·Rechargeable Penile Rigidity Device.
EDP
FDA UDI
REACH MEDICAL, INC.·00850004857113·Manual Penile Rigidity Device.
EDP
FDA UDI
REACH MEDICAL, INC.·00850004857045·External Penile Rigidity Device Manually Operated
EDP
FDA UDI
REACH MEDICAL, INC.·00850004857052·External Penile Rigidity Device Battery Operated
Penile Adjustable Loop
FDA UDI
REACH MEDICAL, INC.·00850004857007·Adjustable penile constriction band that can be...
HONEYWELL
FDA Adverse Event
Injury
·KAZ USA, INC., A HELEN OF TROY COMPANY·Product code KFZ·June 9, 2022
HONEYWELL
FDA Adverse Event
Injury
·KAZ USA, INC., A HELEN OF TROY COMPANY·Product code KFZ·December 5, 2018
WALGREENS
FDA Adverse Event
Injury
·KAZ USA, INC., A HELEN OF TROY COMPANY·Product code KFZ·January 28, 2022
BALLARD CS NEO/PED, 6 FR, Y-ADAPTER
FDA Adverse Event
Injury
·AVANOS MEDICAL INC.·Product code BSY·February 3, 2022
VICKS
FDA Adverse Event
Injury
·KAZ USA, INC., A HELEN OF TROY COMPANY·Product code KFZ·December 16, 2022
CADD CASSETTE
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code LHI·December 3, 2020
VICKS
FDA Adverse Event
Injury
·KAZ USA, INC., A HELEN OF TROY COMPANY·Product code KFZ·October 28, 2016
WALGREENS
FDA Adverse Event
Malfunction
·KAZ USA, INC., A HELEN OF TROY COMPANY·Product code KFZ·April 20, 2020
VICKS
FDA Adverse Event
Injury
·KAZ USA, INC., A HELEN OF TROY COMPANY·Product code KFZ·April 3, 2020
VICKS
FDA Adverse Event
Injury
·KAZ USA, INC., A HELEN OF TROY COMPANY·Product code KFZ·March 13, 2019
FRESENIUS DIALYSIS DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code FIL·July 24, 2002
DESTINO¿ REACH STEERABLE GUIDING SHEATH
FDA Adverse Event
Injury
·OSCOR INC.·Product code DYB·November 12, 2025
BALLARD CLOSED SUCTION ADULT, 12 FR, DSE
FDA Adverse Event
Injury
·Product code BSY·November 19, 2020