Device typeEndoscopic-access dilator, single-use: A device intended to be used to dilate a body lumen or access channel to facilitate the introduction of endoscopic instruments percutaneously (through the skin) or through a natural orifice (e.g., urethra). It may be a flexible or rigid rod/tube with a tapered distal tip. This is a single-use device.
FDA categoryDILATOR, URETHRAL
Device ID00827002460751
Catalog numberFUS-095035-DL
AvailabilityPrescription
Single useYes
SterileYes
MRI safetyLabeling does not contain MRI Safety Information