9 results
·
18ms
·
Sources: EU EUDAMED, US FDA
ET-RESTRAINT CAT. # ER 4000
FDA 510(k)
FDA Class 1
·Anesthesiology
3M™ Unitek™
FDA UDI
3M COMPANY·30605861027893·3M™ Unitek™ Stainless Steel Second Primary Mola...
ARROW
FDA UDI
TELEFLEX INCORPORATED·10801902140873·Pediatric Two-Lumen Central Venous Catheterizat...
DIMENSION VISTA AFP FLEX REAGENT CARTRIDGE, MODEL 6454
FDA 510(k)
FDA Class 2
·Immunology
SYNERGY VLS CAP NUT MODELS 2206, 6102
FDA 510(k)
FDA Class 2
·Orthopedic
LINER: CC E CC LIGHT FLAT PE HC LINER Ø 32 / E
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·October 30, 2019
UNKNOWN ALPS RADIAL HEAD PLATE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code HRS·June 27, 2014
INFUSOMAT SPACE - US VERSION
FDA Adverse Event
Malfunction
·B. BRAUN MELSUNGEN AG·Product code FRN·November 19, 2012
ACCU-CHEK FLEXLINK PLUS
FDA Adverse Event
Injury
·ROCHE INSULIN DELIVERY SYSTEMS INC·Product code FPA·November 10, 2010