38 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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GenCut Core Biopsy System
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
FLEXOR SHUTTLE TIBIAL GUIDING SHEATH
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·September 29, 2020
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·September 15, 2020
PRADO™ Lumbar Interbody Fusion System
FDA UDI
Pt. Solutions, LLC·G616RAFS142839060·NON-STERILE PLANAR, PRADO A SYMMETRIC PEEK IBFD...
APPLIANCE, FIXATION, SPINAL INTERLAMINAL
FDA Adverse Event
Injury
·SYNTHES USA·Product code KWP·March 31, 2016
C-PET PLUS IMAGING SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
SPIDER STANDARD AND ADVANCED
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
FLEXOR RTPS GUIDING SHEATH
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·February 27, 2020
LAMITRODE TRIPOLE 16C
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 24, 2013
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 30, 2014
3002 SECURE II
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·June 20, 2011
FLEXOR SHUTTLE TIBIAL GUIDING SHEATH
FDA Adverse Event
Injury
·COOK INC·Product code DYB·October 29, 2025
FLEXOR SHUTTLE TIBIAL GUIDING SHEATH
FDA Adverse Event
Injury
·COOK INC·Product code DYB·October 29, 2025
DYB INTRODUCER, CATHETER
FDA Adverse Event
Injury
·COOK INC·Product code DYB·November 12, 2025
FLEXOR SHUTTLE SELECT GUIDING SHEATH
FDA Adverse Event
Injury
·COOK INC·Product code DYB·October 29, 2025
FLEXOR SHUTTLE TIBIAL GUIDING SHEATH
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·January 12, 2018
FLEXOR HIGH-FLEX ANSEL GUIDING SHEATH
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·March 3, 2020
THAL-QUICK CHEST TUBE SET
FDA Adverse Event
Malfunction
·COOK INC·Product code GBX·January 7, 2020
FLEXOR ANSEL GUIDING SHEATH
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·March 3, 2020
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·January 10, 2022