Kyphoplasty systems
Impix-Manta
A collection of various orthopaedic surgical instruments, dressings and the necessary materials intended to be used to perform an orthopaedic surgical procedure, however the kit is not dedicated to orthopaedic implantation. It does not contain pharmaceuticals. This is a reusable device.
Where to buy Impix-Manta
We do not have contact details for Medicrea International yet. Send a request and we will route it to the right person for your country.
Impix-Manta 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 |
|---|---|---|---|
| A20120003 | — | Not stated | Available |
| A20120004 | — | Not stated | Available |
| A20150006 | — | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is Impix-Manta used for?
A collection of various orthopaedic surgical instruments, dressings and the necessary materials intended to be used to perform an orthopaedic surgical procedure, however the kit is not dedicated to orthopaedic implantation. It does not contain pharmaceuticals. This is a reusable device.
Who makes Impix-Manta?
Impix-Manta is made by Medicrea International. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does Impix-Manta come in?
The FDA device database does not list sizes for Impix-Manta. Check the instructions for use or ask a Medicrea International representative.
Is Impix-Manta MRI safe?
The FDA device database entry for Impix-Manta does not state its MRI safety status. Check the labeling before MRI.
Is Impix-Manta FDA cleared?
Impix-Manta is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Medicrea International sales representative?
Medicrea International has not listed representatives on LA Vascular yet. Visit the Medicrea International 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.