Kyphoplasty systems
PureKit Syringe MV
by Teknimed
A collection of sterile surgical instruments, tools, and materials designed to prepare and apply bone cement during an orthopaedic surgical procedure (e.g., hip replacement, arthroplasty, or vertebroplasty). It typically includes items such as forceps, a mallet, cement delivery injectors, delivery tubes, and mixing devices; it may or may not include bone cement. This is a single-use device.
Where to buy PureKit Syringe MV
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PureKit Syringe MV 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 |
|---|---|---|---|
| T060426MV | — | Not stated | Available |
| T060428MV | — | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is PureKit Syringe MV used for?
A collection of sterile surgical instruments, tools, and materials designed to prepare and apply bone cement during an orthopaedic surgical procedure (e.g., hip replacement, arthroplasty, or vertebroplasty). It typically includes items such as forceps, a mallet, cement delivery injectors, delivery tubes, and mixing devices; it may or may not include bone cement. This is a single-use device.
Who makes PureKit Syringe MV?
PureKit Syringe MV is made by Teknimed. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does PureKit Syringe MV come in?
The FDA device database does not list sizes for PureKit Syringe MV. Check the instructions for use or ask a Teknimed representative.
Is PureKit Syringe MV MRI safe?
The FDA device database entry for PureKit Syringe MV does not state its MRI safety status. Check the labeling before MRI.
Is PureKit Syringe MV FDA cleared?
PureKit Syringe MV is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Teknimed sales representative?
Teknimed has not listed representatives on LA Vascular yet. Visit the Teknimed 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.