1,352 results
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36ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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AMBI, INC.
FDA registration
AMBI, INC.·5 products·🇺🇸 United States
Inject-Ease
FDA UDI
AMBI, INC.·00025294874007·Holder for disposable syringes that hides the n...
INJECT-EASE
FDA Adverse Event
Injury
·AMBIMEDINC / AMBI, INC.·Product code KZH·December 5, 2025
INJECT-EASE
FDA Adverse Event
Malfunction
·AMBIMEDINC / AMBI, INC.·Product code KZH·December 5, 2025
STROLLER G3 PB
FDA Adverse Event
Other
·CAIRE, INC.·Product code BYJ·April 8, 2008
PERFUSOR
FDA Adverse Event
Death
·B. BRAUN MELSUNGEN AG·Product code FRN·August 20, 2020
AMBI-COMPRESSION HIP SCREW
FDA Adverse Event
Injury
·SMITH & NEPHEW·Product code KTT·February 2, 2002
PERFUSOR SPACE
FDA Adverse Event
Injury
·B. BRAUN MELSUNGEN AG·Product code FRN·December 20, 2022
AMI INC.
FDA registration
AMI INC.·1 product·🇰🇷 South Korea
PICO LEGEND
FDA UDI
AMI Inc.·08800042100292·
BIOXEL
FDA UDI
AMI Inc.·08800042100018·
Q-MASTER
FDA UDI
AMI Inc.·08800042100001·
AMBU SPUR II ADULT RESUSCITATOR
FDA Adverse Event
Malfunction
·Product code BTM·January 29, 2013
AMBU INC.
FDA Adverse Event
Malfunction
·AMBU, INC.·Product code BTM·February 7, 2012
SPUR II
FDA Adverse Event
Malfunction
·AMBU A/S·Product code BTM·March 25, 2010
DREAMSTATION AUTO CPAP
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·October 17, 2023
AMBU SPUR II PEDIATRIC RESUSCITATOR
FDA Adverse Event
Malfunction
·AMBU A/S·Product code OEV·July 2, 2025
AMBU SPUR II PEDIATRIC RESUSCITATOR
FDA Adverse Event
Malfunction
·AMBU A/S·Product code OEV·July 2, 2025
DREAMSTATION AUTO CPAP
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·October 19, 2023
DREAMSTATION AUTO BIPAP
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 4, 2025