PINECY® Kyphoplasty Tool Kit

Primary DI

06935456209148

Basic UDI-DI Code

69354562PLYL08XR

Reference

FA08401

Device Types

Single use Sterile

Regulation

Eu Mdr

Classification

Eu Md Class 2a

Status

On The Market

Manufacturer

Princeton Medical Scientific Co.,Ltd

The Kyphoplasty Tool Kit expectations for clinical implementation of percutaneous vertebral plasty or protruding after percutaneous vertebral plasty and one-time use of minimally invasive surgery.There are 304 stainless steel,30Cr13 stainless steel and ABS,PC,PA,TPUcomponents. The retention time usually does not exceed 2 hours.

The Basic UDI-DI associated with this device has 38 devices in total. Below are some other devices sharing the same Basic UDI-DI.

Other on-the-market devices with the same classification (Eu Md Class 2a) and regulation (EU MDR).