Atherectomy
Peripheral ROTAPRO
by Boston Scientific Corporation
An assembly of devices intended to mechanically disrupt/remove atheroma plaque from the walls of coronary arteries. It typically includes a mains electricity (AC-powered) energy-producing generator with monitoring functions, a remote control or foot-switch, a handpiece (to which the catheter connects) and a dedicated disposable catheter with a cutting or abrasive head that transmits the mechanical energy to the atheroma. The system may include an integrated irrigation/suction system and includes/requires accessory devices for its function (e.g., saline/lubricant, pump, guidewire).
Peripheral ROTAPRO models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| H749395141250 | Atherectomy Rotating Component Diameter 1.25 mm | Not stated | Available |
| H749395141500 | Atherectomy Rotating Component Diameter 1.50 mm | Not stated | Available |
| H749395141750 | Atherectomy Rotating Component Diameter 1.75 mm | Not stated | Available |
| H749395142000 | Atherectomy Rotating Component Diameter 2.00 mm | Not stated | Available |
| H749395142150 | Atherectomy Rotating Component Diameter 2.15 mm | Not stated | Available |
| H749395142250 | Atherectomy Rotating Component Diameter 2.25 mm | Not stated | Available |
| H749395142380 | Atherectomy Rotating Component Diameter 2.38 mm | Not stated | Available |
| H749395142500 | Atherectomy Rotating Component Diameter 2.50 mm | Not stated | Available |
Procedures that use atherectomy
Frequently asked questions
What is Peripheral ROTAPRO used for?
An assembly of devices intended to mechanically disrupt/remove atheroma plaque from the walls of coronary arteries. It typically includes a mains electricity (AC-powered) energy-producing generator with monitoring functions, a remote control or foot-switch, a handpiece (to which the catheter connects) and a dedicated disposable catheter with a cutting or abrasive head that transmits the mechanical energy to the atheroma. The system may include an integrated irrigation/suction system and includes/requires accessory devices for its function (e.g., saline/lubricant, pump, guidewire).
Who makes Peripheral ROTAPRO?
Peripheral ROTAPRO is made by Boston Scientific Corporation. It is listed under atherectomy devices in our device library.
What sizes does Peripheral ROTAPRO come in?
Sizes listed for Peripheral ROTAPRO: Atherectomy Rotating Component Diameter: 1.25–2.5 mm. Confirm availability with the manufacturer's instructions for use.
Is Peripheral ROTAPRO MRI safe?
The FDA device database entry for Peripheral ROTAPRO does not state its MRI safety status. Check the labeling before MRI.
Is Peripheral ROTAPRO FDA cleared?
Peripheral ROTAPRO is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Boston Scientific Corporation sales representative?
Boston Scientific Corporation has not listed representatives on LA Vascular yet. Visit the Boston Scientific Corporation company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.