Eu Mdr Eu Md Class 3 On The Market

PLASMA-X PRP

The device is made to prepare platelet rich plasma. The device separates red blood cell from whole blood after centrifugation and adjust amount of plasma. This results in increase of platelet counts.

Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0

Basic Information

Primary DI
16429811388021
Basic UDI-DI Code
6429811388PXA30IH9
Reference
PXA-30
Device Types
Sterile
Regulation
Eu Mdr
Classification
Eu Md Class 3
Status
On The Market

Additional Description

PLASMA-X is the all-in-one kit consisting of a series of disposable devices that allow the production and application of autologous blood components for non-transfusion use. It was designed to obtain the maximum possible concentration of PRP with a single centrifugation with the great advantage of reducing preparation times. The separation device (PRO-PRP P30A), which allows a clear view of the blood components and an easy and safe collection of the PRP in the syringe, complies with the regulations of CE class III medical devices. PLASMA-X requires the use of a centrifuge.

Medical Purpose

The device is made to prepare platelet rich plasma. The device separates red blood cell from whole blood after centrifugation and adjust amount of plasma. This results in increase of platelet counts.

CND Nomenclature Codes

Code Description
B010202 PLATELETS CONCENTRATE TRANSFER BAGS AND KITS

Similar Devices

Other on-the-market devices with the same classification (Eu Md Class 3) and regulation (EU MDR).

View all