Precision Medical Technologies, Inc. has received the results of its PEEK cell’s cleaning validation. All test method acceptance criteria was met. Premedtec earned an extraction efficiency percentage of 87% on the “Quantification of Extractable Residue by Gravimetric Analysis Final Report”. The standard used for this test method (ASTM F2459) requires the extraction efficiency to be greater than 75%. A bioburden test was completed and showed that bioburden is not of high concern on Premedtec’s devices. Going forward cytotoxicity will be tested on a quarterly basis.
