18 results · 22ms · Sources: EU EUDAMED, US FDA

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AP 50/30 Insufflator with Insuflow Port

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

FORTRESS INTRODUCER SHEATH SYSTEM MODEL 358813, 358814, 358815

FDA 510(k)
FDA Class 2 ·Cardiovascular

MODULARIS VARIOSTAR

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

CRE PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·March 31, 2025

CRE PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·June 11, 2025

CRE PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·May 30, 2025

CRE PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·March 5, 2025

CRE PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·June 5, 2025

CRE PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·January 28, 2025

CRE PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·July 28, 2025

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 14, 2013

3 MOTOR ADVANCE BED

FDA Adverse Event
Malfunction ·HILL-ROM INC.·Product code FNL·June 22, 2011

TENNACULUM FORCEPS INSTRUMENT

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL, INC·Product code GCJ·September 12, 2008

I-STAT CHEM8+ CARTRIDGE (SEE H10 FOR EC8+)

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE·Product code JGS·October 7, 2017

CRE PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·September 30, 2025

CRE PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·May 12, 2025

CRE PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·January 10, 2025

FORTRESS INTRODUCER SHEATH SYSTEM - 6FR, 45CM

FDA Adverse Event
Malfunction ·CONTRACT MEDICAL INTERNATIONAL GMBH·Product code DYB·November 30, 2015