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2014-01-20
20140120 Safety Information
Medical standards apply IEC/EN/ES60601-1 equipment, how to decide whether patients
need to be designed to protect the product level (MOPP) or operator (eg health care)
protection class (MOOP)?
In the medical product legislation will be divided into patient protection class level of
protection (MOPP) and operator protection level (MOOP) two kinds, and the negative of
the desired design, production costs are different, in the initial application thought into
the medical market power supply manufacturers often can not decide what they want to
design grade products, there is a clear explanation of this part of the regulations in the
medical device products will be used when the patient environment (PATIENT
ENVIRONMENT) area must comply with disease risk level of protection (MOPP), so
manufacturers can design a criteria to decide what level of products, which respond to
market customers.
Patient Environment (PATIENT ENVIRONMENT) as defined in the standard
In view of the power supply terminal manufacturers are often unable to confirm the
application of medical products, so now most of the power supply manufacturers will
adopt application MOPP way, backward compatibility MOOP, to avoid end-customers
can not use MOOP design issues.
need to be designed to protect the product level (MOPP) or operator (eg health care)
protection class (MOOP)?
In the medical product legislation will be divided into patient protection class level of
protection (MOPP) and operator protection level (MOOP) two kinds, and the negative of
the desired design, production costs are different, in the initial application thought into
the medical market power supply manufacturers often can not decide what they want to
design grade products, there is a clear explanation of this part of the regulations in the
medical device products will be used when the patient environment (PATIENT
ENVIRONMENT) area must comply with disease risk level of protection (MOPP), so
manufacturers can design a criteria to decide what level of products, which respond to
market customers.
Patient Environment (PATIENT ENVIRONMENT) as defined in the standard
In view of the power supply terminal manufacturers are often unable to confirm the
application of medical products, so now most of the power supply manufacturers will
adopt application MOPP way, backward compatibility MOOP, to avoid end-customers
can not use MOOP design issues.
