Surgical planning POWER OM

By

45 Ncm
RECOMMENDED IMPLANT INSERTION TORQUE
sterilised by beta rays
sterilise
printed on the box allows to display the surgical protocol
the QR code
with the standards set by the MDR 2017/745
packaging process
top is carefully washed and dried.
The methacrylate vial with Polyethylene (PE)
are supplied in two separate kits based on the drill diameter
Drill stops

More Details

all informations about this product

“For inquiries regarding pricing and product availability, please contact us.”

We at DiarTajhiz proudly operate as one of the most reputable suppliers and importers of dental equipment, especially dental implant equipment.

With over 12 years of experience in the dental industry and collaboration with top international brands, our effort is always to provide quality products that meet global standards to the Iranian dental community. Our goal is to create trust and satisfaction among customers by providing original products and professional services.

 

 

 

 

 

Surgical Protocol

The Power surgical protocol was developed to provide
surgeons with indications on how to choose the most suitable
instruments for implant site preparation, depending on the
type of bone.
However, it is the duty of the surgeon to apply the most
appropriate surgical protocol on the basis of his/her experience
and following a thorough assessment of the clinical situation
of the individual patient.
For the preparation of the implant site, IML has developed
cylindrical drills with a tapered tip and depth marks in
accordance with the length of the implant; they can be used
with drill stops.

RECOMMENDED IMPLANT INSERTION
TORQUE: 45 Ncm

 

 

Packaging

IML packaging process is performed in compliance with the standards set by the MDR 2017/745 Directive, which
guarantee the sterilisation shelf-life.

All the IML implants are sterilised by beta rays.
Implants are packaged in a vial that, in turn, is placed inside a plastic container closed by a cap with safety seal and
bearing a label with the identification data of the implant. Then the plastic container is placed inside a cardboard
box bearing the same label. Further two copies of the label are into the cardboard box, to be placed on the implant
passport and on the patient’s medical record sheet

 

 

 

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