26 results
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23ms
·
Sources: EU EUDAMED, US FDA
CELL-DYN 1800 SYSTEM
FDA 510(k)
FDA Class 2
·Hematology
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526827851·***DISC*LEVAMED ANKLE SUPPORT BLACK III
Latitude™ EV
FDA UDI
TORNIER, INC.·00846832002887·Humeral Stem - Coated
Symmetry Surgical
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482043707·Symmetry® Scissors, Operating, Curved, Sharp/Sh...
NA
FDA UDI
STRYKER CORPORATION·07613153001423·5.0mm Round Solid Carbide Bur Extra Long
TAXOL ADMINISTRATION SET
FDA 510(k)
FDA Class 2
·General Hospital
MODIFICATION TO EBI SPINELINK ANTERIOR CERVICAL SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
21GX.75IN. BD VACUTAINER® WINGED SAFETY PBBCS WITH 12 IN TUBING
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code JKA·November 27, 2017
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·February 5, 2024
BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET PRE-ATTACHED HOLDER 23G NEEDLE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·December 3, 2017
BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·January 31, 2024
ASR UNI FEMORAL IMPL SIZE 45
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·April 2, 2013
FIRST PICC KIT W/ INTROSYTE-N INTRODUCER
FDA Adverse Event
Malfunction
·ARGON MEDICAL DEVICES, INC.·Product code LJS·March 22, 2011
AED PLUS
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORP·Product code MKJ·April 16, 2008
LOGIC TIB INSERT IMPL CRC, SZ 4, 11MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·January 3, 2023
BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code FPA·April 3, 2024
BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code FPA·February 28, 2024
Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x35 mm Catalog Number: 18965035S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.
FDA Enforcement
Class II
·Terminated·Stryker GmbH·June 24, 2020
BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code FPA·January 18, 2024
BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code FPA·December 14, 2023