Катетер проводниковый CEREBASE DA, исполнения:

Страна: Беларусь

Язык: русский

Источник: Министерством здравоохранения Республики (Центр экспертиз и испытаний в здравоохранении)

Доступна с:

Medos International SARL, ШВЕЙЦАРИЯ

класс:

изделия медицинского назначения

Производитель:

Medos International SARL

Дата Авторизация:

2021-06-24

Характеристики продукта

CEREBASE DA Guide Sheath
LCN 208918-001/A
© 2020 Cerenovus.
All rights reserved.
Printed 01/20
Medos International SÀRL
Chemin-Blanc 38, 2400
Le Locle, Switzerland
2
ENGLISH
IMPORTANT INFORMATION
Please Read Before Use
CEREBASE DA Guide Sheath
Description
The CEREBASE DA Guide Sheath package contains the guide sheath,
a hemostasis valve, and a dilator.
The CEREBASE DA Guide Sheath is a single lumen, variable stiffness
guide sheath. It has a radiopaque marker band on the distal end
and a luer hub at the proximal end. The guide sheath has an outer
hydrophilic coating on the distal 20 cm that reduces friction during
use. The lubricious PTFE lined inner lumen is designed to facilitate
delivery of guide wires, catheters, and other devices. Please refer to
the label for short sheath compatibility.
The dilator is a single lumen radiopaque catheter with a tapered
distal
end and a luer hub at the proximal end. The dilator is compatible with
the CEREBASE DA Guide Sheath and up to 0.038 inch diagnostic
guidewires. The dilator facilitates the percutaneous transition from
the
skin through the subcutaneous tissue to the vessel.
Indications
The CEREBASE DA Guide Sheath is indicated for the introduction of
interventional devices into the neuro vasculature.
Contraindications
None known.
WARNINGS
•
The CEREBASE DA Guide Sheath should only be used by
physicians trained in neuro interventional endovascular
procedures at medical facilities with the proper imaging
equipment.
•
Do not use with Ethiodol or Lipiodol contrast media, or other
such contrast media which incorporates the components of these
agents.
•
Do not advance or withdraw an intravascular device against
resistance until the cause of the resistance is determined by
fluoroscopy. Movement of the device against resistance may
cause vessel injury or damage to the device.
•
Discard the sheath after one procedure. Structural integrity and/or
function may be impaired through reuse or cleaning. This device
is extremely difficult to clean after exposure to biological mat