13 results
·
28ms
·
Sources: EU EUDAMED, US FDA
VIRATEST-DIA(TM) MEASLES (RUBEOLA)
FDA 510(k)
FDA Class 1
·Microbiology
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756349697·CYSTO PACK
Gen. Acces/ Instr. Tip Guard
FDA UDI
KATENA PRODUCTS, INC.·00841668112359·SURG-I-BAND PURPLE GLOW
Gen. Acces/ Instr. Tip Guard
FDA UDI
KATENA PRODUCTS, INC.·00841668112267·SURG-I-BAND ORANGE
AltiVate Reverse Humeral Stem, 48mm
FDA 510(k)
FDA Class 2
·Orthopedic
EXETER HIP STEM
FDA 510(k)
FDA Class 2
·Orthopedic
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·July 12, 2024
CUP: MPACT ACETABULAR SHELL 56 MULTI-HOLE
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LPH·March 15, 2021
LINER: MPACT FLAT PE HC 36/F
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LPH·June 24, 2021
LINER: MPACT FLAT PE HC LINER 36/F
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LPH·August 27, 2020
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·November 30, 2010
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER MANUFACTURING FACILITY·Product code KDJ·July 2, 2014
RECOVERY ROOM STRETCH
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FPO·December 19, 2012