Piezotome® M+

Piezotome® M+

The ultrasonic expert for fast and secure bone surgery

Piezotome® M+ is a versatile device. Its dual connection allows you to connect two handpieces thus enabling faster clinical procedures. Easy adjustment settings with its touch screen and multifunction footswitch for perfect control throughout the surgical procedure.



01 PRODUCT BENEFITS

SELECTIVE CUT

Safe and atraumatic ultrasonic piezo bone surgery. Non active on fragile anatomic structure (Piezo modulated mode). 

NEWTRON® TECHNOLOGY

Patented technology electronics to provide great efficacy and clinical benefits. 

VERSATILE

Dedicated to ultrasonic precise bone surgery the Piezotome® M+ has:
- a dual connection for faster surgery
- a tactile screen for intuitive settings 

02 MAIN CHARACTERISTICS

PRESERVATION

Bone preservation thanks to highly precise cut, linear tip vibrations, controlled and regular tip amplitude.

EFFICACY

Boosted Piezotome® handpiece with 6 ceramic rings for safe and atraumatic bone surgery.

Automatic frequency adjustment for optimal and continuous efficiency irrespective of the load applied. 

Automatic power regulation for constant performance even in dense bone.

COMFORT

For both surgeon and patient: safe and effortless cut, increased tactile sensation and reduced post-operative pain with less swelling and bruising. 

PROVEN ULTRASONIC CLINICAL BENEFITS

- Tissue preservation (nerves, arteries, dura mater)
- Thin and precise osteotomies
- Reduced post-operative pain 
- Better healing 
- Stable and long term results 

TOTAL CONTROL

- Multifunction ON/OFF footswitch OR certified IPX8
- Precise and constant irrigation flow rate to avoid bone necrosis 
- Single use irrigation lines for perfect asepsis
- Long-lasting durable components: handpiece, wrench, sterilization tray

WIDE RANGE OF SPECIFICALLY DESIGNED TIPS

- M+ tips are designed to respect patients anatomy and to meet surgeons need in terms of robustness
- Tips are supplied single use or 5 times reusable

05 TESTIMONIALS

07 LEGAL NOTICE

These medical devices are Class IIb according to the applicable European Directive in force.
They carry CE marking. Notified body: LNE-GMED 0459.
These medical devices are reserved for health personnel. They are not reimbursed by health insurance organisations.
This equipment has been designed and manufactured in accordance with an EN ISO 13485-certified quality assurance system. Read the user manual, available on the manufacturer’s website, carefully. SATELEC® (France).
Manufactured by SATELEC® (FRANCE) distributed by COMEG.