81 results · 23ms · Sources: EU EUDAMED, US FDA

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CONTURA CAVITY MAINTENANCE CATHETER

FDA 510(k)
FDA Class 2 ·Radiology

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04047872673150·LEVAMED STABILI-TRI ANK SUP BLU L III

BIPAP SYNCHRONY VENTILATORY SUPPORT SYSTEM

FDA 510(k)
FDA Class 2 ·Anesthesiology

ADVANCED UROSCIENCE INJECTION NEEDLE

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

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 10, 2025

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 5, 2025

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 13, 2026

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 14, 2026

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 18, 2026

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 19, 2025

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 19, 2025

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 8, 2025

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·March 30, 2026

LINEAR? ST

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·February 20, 2026

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·March 31, 2026

GORE INTRODUCER SHEATH WITH SILICONE PINCH VALVE

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code DYB·April 25, 2013

8800

FDA Adverse Event
Malfunction ·GE MED SYSTEMS (INDIA) PRIVATE LTD (GE PRIVATE)·Product code JAA·April 27, 2011

PUMP MMT-722LNAS PRDGM INS SK EN ML

FDA Adverse Event
Injury ·MEDTRONIC MINIMED·Product code LZG·August 1, 2008

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 6, 2026

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 14, 2026