Loading ...
Loading ...
Loading ...
BD-S / BD-S-UL, ED-S / ED-S-UL, FD-S / FD-S-UL (E1) 10/2020 page 9/59
DANGER
Electrical hazard.
Danger of death.
∅ The chamber must NOT become wet during operation or maintenance.
The chambers were produced in accordance with VDE regulations and were routinely tested in accord-
ance to VDE 0411-1 (IEC 61010-1).
During and shortly after operation, the temperature of the inner surfaces almost equals the set-point.
CAUTION
The glass doors and glass door handles (BD-S / BD-S-UL), inner chamber, exhaust
air flap, door window (option), and the door gaskets will become hot during opera-
tion.
Danger of burning.
∅ Do NOT touch the glass doors, inner surfaces, exhaust air flap, door window, access
ports, door gaskets, or the charging material during operation.
∅ FD-S / FD-S-UL: Do not place the power cable over the door gap when the chamber is
hot after operation.
1.6 Intended use
The chambers are suitable for exact tempering of harmless materials and for drying and heat treatment of
solid or pulverized charging material, as well as bulk material, using the supply of heat. They can be used
to dry e.g. glassware, and for warm storage of liquids in containers.
Because of their precise temperature accuracy the incubators BD-S / BD-S-UL are especially useful for
incubation of cultures at a standard temperature of 37 °C / 98.6 °F.
A solvent content must not be explosive or flammable. A mixture of any component of the charging mate-
rial with air must NOT be explosive. The operating temperature must lie below the flash point or below the
sublimation point of the charging material. Any component of the charging material must NOT be able to
release toxic gases.
Other applications are not approved.
The chambers are not classified as medical devices as defined by the Medical Device Directive
93/42/EEC.
Do NOT use the chamber for drying processes when large quantities of vapor would form and result in
condensation.
Due to the special demands of the Medical Device Directive 93/42/EEC, these ovens are not
qualified for sterilization of medical devices as defined by the directive.
Observing the instructions in this operating manual and conducting regular maintenance work
(chap. 13) is part of the intended use.
WARNING: If customer should use a BINDER chamber running in non-supervised continu-
ous operation, we strongly recommend in case of inclusion of irrecoverable specimen or
samples to split such specimen or samples and store them in at least two chambers, if this is
feasible.
The charging material shall not contain any corrosive ingredients that may damage the ma-
chine components. Such ingredients include in particular acids and halides. Any corrosive
damage caused by such ingredients is excluded from liability by BINDER GmbH.
Loading ...
Loading ...
Loading ...