Kyphoplasty systems
BiMobile Dual Mobility System - Instruments
by WALDEMAR LINK GmbH & Co. KG
A non-powered, hand-held, surgical instrument designed to transmit impact forces, typically from a hammer/mallet to an orthopaedic implant (e.g., intramedullary nail or stem), to position/drive the implant into the body during impact-based implantation. It commonly includes an impact-absorbing handle with a distal end shaped to conform to the implant (i.e., flat or anatomically curved). This is a reusable device.
Where to buy BiMobile Dual Mobility System - Instruments
We do not have contact details for WALDEMAR LINK GmbH & Co. KG yet. Send a request and we will route it to the right person for your country.
BiMobile Dual Mobility System - Instruments 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 |
|---|---|---|---|
| 184-135/12 | — | Not stated | Available |
| 184-136/12 | — | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is BiMobile Dual Mobility System - Instruments used for?
A non-powered, hand-held, surgical instrument designed to transmit impact forces, typically from a hammer/mallet to an orthopaedic implant (e.g., intramedullary nail or stem), to position/drive the implant into the body during impact-based implantation. It commonly includes an impact-absorbing handle with a distal end shaped to conform to the implant (i.e., flat or anatomically curved). This is a reusable device.
Who makes BiMobile Dual Mobility System - Instruments?
BiMobile Dual Mobility System - Instruments is made by WALDEMAR LINK GmbH & Co. KG. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does BiMobile Dual Mobility System - Instruments come in?
The FDA device database does not list sizes for BiMobile Dual Mobility System - Instruments. Check the instructions for use or ask a WALDEMAR LINK GmbH & Co. KG representative.
Is BiMobile Dual Mobility System - Instruments MRI safe?
The FDA device database entry for BiMobile Dual Mobility System - Instruments does not state its MRI safety status. Check the labeling before MRI.
Is BiMobile Dual Mobility System - Instruments FDA cleared?
BiMobile Dual Mobility System - Instruments is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a WALDEMAR LINK GmbH & Co. KG sales representative?
WALDEMAR LINK GmbH & Co. KG has not listed representatives on LA Vascular yet. Visit the WALDEMAR LINK GmbH & Co. KG 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.