8 results
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18ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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PROCLAIM¿ DRG IMPLANTABLE PULSE GENERATOR
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·August 5, 2019
INSIGNIA
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 3, 2014
ORBERA365 INTRAGASTRIC BALLOON SYSTEM
FDA Adverse Event
Injury
·APOLLO ENDOSURGERY, INC.·Product code LTI·May 15, 2019
ORBERA365 INTRAGASTRIC BALLOON SYSTEM
FDA Adverse Event
Injury
·APOLLO ENDOSURGERY, INC.·Product code LTI·June 12, 2019
ORBERA365 INTRAGASTRIC BALLOON SYSTEM
FDA Adverse Event
Injury
·APOLLO ENDOSURGERY, INC.·Product code LTI·June 11, 2019
ORBERA365 INTRAGASTRIC BALLOON SYSTEM
FDA Adverse Event
Injury
·APOLLO ENDOSURGERY, INC.·Product code LTI·June 12, 2019
ORBERA365 INTRAGASTRIC BALLOON SYSTEM
FDA Adverse Event
Injury
·APOLLO ENDOSURGERY, INC.·Product code LTI·September 20, 2019
ORBERA365 INTRAGASTRIC BALLOON SYSTEM
FDA Adverse Event
Injury
·APOLLO ENDOSURGERY, INC.·Product code LTI·September 20, 2019