PS200-040 – Medtronic PEAK PlasmaBlade 4.0

About the Medtronic PEAK PlasmaBlade 4.0 — SKU PS200-040

SKU PS200-040 corresponds to the Medtronic PEAK PlasmaBlade 4.0 from Medtronic, manufactured by MEDTRONIC NAVIGATION, INC. According to its FDA GUDID device record, this item is described as “Plasmablade x ps200-040 4.0 green”. We include this FDA-sourced identification alongside the standard catalog details so purchasing and receiving teams can verify the exact device before it ships.

Product Details

The Medtronic PEAK PlasmaBlade 4.0 is a single-use surgical device that uses pulsed plasma-mediated radiofrequency energy to cut tissue and coagulate bleeding with reduced thermal spread compared to conventional electrosurgery. Its 4.0 mm blade tip is designed for precise dissection through subcutaneous tissue planes. It is intended for use with compatible Medtronic PlasmaBlade generators.

When comparing this item to similar products from other manufacturers, use SKU PS200-040 to confirm you’re matching the exact configuration your facility needs.

PS200-040 Ordering & Compatibility

For reordering and inventory matching, use the SKU shown on this page. FDA records list this item’s commercial-distribution status as In Commercial Distribution. The FDA record also indicates this device is single-use, sterile, though packaging and dating should always be verified on the physical unit received. Reach out if you need help confirming compatibility with your existing equipment or want to explore backorder alternatives.

If SKU PS200-040 is currently on backorder elsewhere, Class 1 Inventory may already have it in stock or know of a comparable substitute within the same category. We work with buyers across Medtronic and other manufacturer lines to keep procurement moving, and we buy back unused surplus inventory as well.

Specifications

• Catalog product name: Medtronic PEAK PlasmaBlade 4.0
• SKU / model: PS200-040
• Brand: Medtronic
• FDA brand name: PlasmaBlade™ X
• Manufacturer: MEDTRONIC NAVIGATION, INC.
• FDA commercial distribution status: In Commercial Distribution
• FDA record indicates single use: Yes
• FDA record indicates sterile: Yes