Drucker Diagnostics 614B Manual do operador - Página 5

Procurar online ou descarregar pdf Manual do operador para Equipamento de laboratório Drucker Diagnostics 614B. Drucker Diagnostics 614B 16 páginas.

WARNING: This device is intended to be operated by properly trained

personnel who have carefully read the operating manual and are

familiar with the function of the device. [Refer to the clinical

laboratory method specified by the specimen receptacle

manufacturer or established by the medical technology for the

products applications.]

WARNING: For the safety of both the operator and service personnel, care

should be taken when using this centrifuge if handling substances that are

known to be toxic, radioactive or contaminated with pathogenic

microorganisms. When Risk Group II materials are used, (as identified in

the World Health Organization "Laboratory Bio-Safety Manual"), a Bio-

Seal should be employed. The Bio-Seal accessory for the model is the non-

aerosol shield cap with appropriate tube holders (contact Drucker

Diagnostics to purchase). In the event that materials of a higher risk group

are being used, more than one level of protection must be provided.

The use of flammable or explosive materials as well as those materials

which have a vigorous chemical reaction is prohibited.

For your safety and the durability of your machine, never transport or

store centrifuge with tube holders inside machine.

ODEL

ESCRIPTION

The Model 614B is a continuous duty centrifuge designed for the small lab

or doctor's office for the purposes of separating laboratory fluids. The unit

is controlled by a mechanical timer settable from 1 to 30 minutes.

Samples can be safely viewed through the transparent lid. In the event

that the lid is opened during a run, the power to the motor is

disconnected.

For warranty information, see page 2 of this manual.

NTENDED

General purpose laboratory centrifuge, intended for the density-based

separation of fluids through centripetal acceleration.

Users should also comply with the specimen receptable manufacturer's

specific instructions for use, in addition to any other protocols established

by the testing organization.

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