1:10 · Spanish audio
Plasmapheresis and longevity
A look at the apheresis circuit and procedure, explained by the medical team.
The GEMMA device is the only therapeutic apheresis platform in Latin America developed and operated by the same medical organization that created it. Developed by Apheresis Technology, a company co-founded by NexusMed's Medical Director.
Conventional therapeutic apheresis requires large equipment, a central venous catheter, and sessions of 3 to 4 hours. GEMMA was designed to remove these limitations without compromising the clinical efficacy of the procedure.
The result is a compact system that operates with peripheral venous access, reduces extracorporeal volume to ~70 ml, and completes each session in 40 to 50 minutes. Every GEMMA unit is operated directly by the NexusMed medical team, with no technical-service intermediaries.

Hemofenix lineage
Patient during a session with a Hemofenix device, the portable generation that preceded GEMMA. The photograph documents the procedure, not clinical outcomes.

Clinical deployment
Record of a portable device in a private room. This photograph documents the care setting, not the device model or clinical outcomes.

Clinical implementation · Boston
Professionals gathered beside a patient and an apheresis circuit during a clinical session in Boston.

Compared to 3–4 hours with conventional systems.
Compared to 400–500 ml with standard equipment.
No central venous catheter in most indications.
Data accumulated across more than 850 centers in a dozen countries.

Every session monitors pressure, flow, and volume in real time. The operator — always a physician from our team — adjusts the parameters based on each patient's individual clinical response. No generic protocols.
Collected plasma
The bag contains material collected during the procedure. Plasma appearance or color alone does not diagnose disease or demonstrate treatment efficacy.

Most apheresis centers depend on rented equipment or outside maintenance. When the equipment fails, treatment is delayed. NexusMed operates with its own technology: maintenance, calibration, and technical support are handled in-house.
The medical team that designed GEMMA is the same one that operates it in every session. That creates a unique clinical feedback loop: data from every procedure directly informs the device's development. Few institutions in the world have that level of integration.
40–50 minutes versus 3–4 hours. Peripheral access versus central catheter. Extracorporeal volume of ~70 ml versus 400–500 ml. Each of these factors reduces the physiological stress of the procedure and improves tolerance, especially in multi-session protocols.
GEMMA is developed by Apheresis Technology, a company founded by the same medical team that leads NexusMed. With an operational presence in more than 850 clinical centers across a dozen countries, Apheresis Technology combines technology development with clinical experience accumulated over more than two decades.
This integration between the device manufacturer and the clinical center that operates it is unusual in the medical field. It allows NexusMed to maintain direct control over the quality of every procedure, refine protocols using real clinical data, and offer a technical continuity that other centers cannot replicate.
Hands-on training
Professionals review the circuit setup together before each procedure, as part of clinical staff training.

Apheresis is not the only element of a NexusMed protocol. GEMMA is integrated into an individualized therapeutic plan that may include regenerative medicine, cell therapy, biomarker evaluation, and subsequent clinical follow-up.
1:10 · Spanish audio
A look at the apheresis circuit and procedure, explained by the medical team.
GEMMA does not replace conventional medical treatments. Its clinical indication is determined in consultation with the specialist physician based on each patient's medical history, biomarkers, and therapeutic goals.
NexusMed archive

Practice, training and real care settings. These photographs document clinical context, not treatment outcomes.
Only a clinical evaluation can determine that. The first step is a consultation with our Medical Director.
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