Kyphoplasty systems

UNID Fusion

by Medicrea International

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.

Ask about this device Where to buy Compare similar devices

Where to buy UNID Fusion

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.

Request this device

Is this your product? Claim Medicrea International to list your reps and distributors by country and receive buyer requests from your territories.

UNID Fusion models and sizes

From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.

Model / catalog no.SizeMRIStatus
A34100040— Not statedAvailable

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.

📬 The IR Device Brief

One email a month: new FDA clearances, recalls and device pages in vascular & interventional radiology.

We'll email you a link to confirm. Unsubscribe any time.

Suggest edits

For manufacturers and their teams. Each field shows what the page says now: add, remove or rewrite anything, and leave the rest as is. LA Vascular reviews every change before it goes live.

About you