Legal analysis: medical equipment scrapping system
Any instrument or equipment that meets one of the following conditions should be scrapped:
Serious damage that can not be repaired;
More than the service life of the basic parts have been seriously damaged, and can not meet the technical indicators after repair;
Seriously outdated technology, energy consumption is too high (exceeding the national standard of more than 20%), low efficiency;
Model has been eliminated, poor performance and can not downgrade users
The main parts and components can not be supplemented and old and dilapidated;
Model has been eliminated, poor performance and can not be downgraded users;
Irrrational design, technology is not passable, the quality of the poor and can not be converted to utilize;
Maintenance costs are too high (a major overhaul of the original value of more than 50%), economically uneconomic;
Serious pollution of the environment, can not be safely operated;
Seriously polluting the environment, can not be safely operated;
Seriously polluting the environment, can not be safely operated. >Serious pollution of the environment, can not be safely operated, no transformation value;
Measurement test failed, mandatory retirement.
Legal basis: "supervision and management of medical devices regulations" Article 26 The applicant, the filer shall prepare an application for registration or for the record of medical devices product technical requirements. Product technical requirements mainly include finished medical devices can be objectively determined functionality, safety indicators and testing methods. Medical devices should be consistent with the registered or filed product technical requirements.