Details
Device typeAmniotic membrane perforator, single-use: A surgical instrument used to rupture the amniotic membrane (i.e., the amnion - the thin, tough membrane that lines the chorion and contains the foetus and the amniotic fluid) to assist in childbirth, without causing injury to the mother or foetus. It is typically long and shaft-like, and terminates in a rounded nose with a sharp hook. It is made of plastic materials, and may be straight or curved to follow the natural contours of the birthing canal into which it is inserted. Amniotic membrane rupture may also be performed using an amniotome or forceps and/or a trocar. This is a single-use device.
FDA categoryAmniotome
Device ID09350902000211
Catalog numberACD01-G
Single useYes
SterileYes
LatexContains natural rubber latex
MRI safetyLabeling does not contain MRI Safety Information