Product Description

CF-Card-Printer

The documentation of the processing measures in the practice is advisable for the complete documented evidence of infection protection measures in the practice or clinic. This documentation is also required as a component of the release of the prepared instruments for application after sterilization.

To complete the documentation with minimal time expenditure, it is advantageous to use the MELAflash CF-Card-Printer.The automatic documentation is offered here for the autoclaves Pro-Class, the Cliniklav 25 as well as the autoclaves of the S-Class series and MELAtronic EN over the standard on-board serial port (RS 232) with the MELAflash CF-Card-Printer as follows:

MELAflash CF-Card for the documentation of the sterilization cycles

Likewise is it also possible to connect the report printer MELAprint 42 at the serial interface of the autoclave.

The documentation of the processing measures in the practice is not only required by the Medical Devices Operator Ordinance, but is also advisable for the complete documented evidence of infection protection measures in the practice or clinic. This documentation is also required as a component of the release of the prepared instruments for application after sterilization.

It’s also possible to connect the autoclave directly with the practice PC.

The MELAnet Box enables network connection (Ethernet) of the MELAG autoclaves of the Pro-Class, S-Class and the Cliniklav 25. They are connected to the serial interface of the autoclave and receive the protocols of all processes and converts them into a network compatible form and then forwards them in the internal network.

You can also digitally document all these records with the MEALview from Melag. The documentation software MELAwin is additionally required for the readout, storing and processing of the records.

The documentation of the sterilization cycles in the practice is advisable for the complete documented evidence of infection protection measures in the practice or clinic. This documentation is also required as a component of the release of the prepared instruments for application after sterilization.