Kyphoplasty systems
UNID Fusion
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.
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Where to buy UNID Fusion
Contact Medicrea International directly; they can quote, ship, or point you to the distributor for your country.
From medicrea.com, checked November 2026.
No reply, or outside their markets? Send us a request and we route it to a rep or distributor for your country.
UNID Fusion 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 |
|---|---|---|---|
| A34100040 | — | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is UNID Fusion 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 UNID Fusion?
UNID Fusion is made by Medicrea International. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does UNID Fusion come in?
The FDA device database does not list sizes for UNID Fusion. Check the instructions for use or ask a Medicrea International representative.
Is UNID Fusion MRI safe?
The FDA device database entry for UNID Fusion does not state its MRI safety status. Check the labeling before MRI.
Is UNID Fusion FDA cleared?
UNID Fusion 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.