Manufacturer
Spiegelberg
(GmbH & Co.) KG
Tempowerkring 4
21079 Hamburg
Germany
Phone: +49-40-790-178-0
Fax: +49-40-790-178-10
Email: info@spiegelberg.de
http://www.spiegelberg.de
0297
CE-marking according to directive 93/42/EEC
Technical alterations reserved.
Spiegelberg:
IAP-Monitor
IAP 32.1
Operating-Instructions
BEDIAP32.1.91 V 2.0 |
© by Spiegelberg (GmbH & Co.) KG, 2003 |
Innovative Measurement Technology for Medicine
9 |
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Pinout of DB 9 Socket |
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1: Uref Input |
6: Uref Output (2,5 V) |
2: RxD |
7: Digital Gnd |
3: TxD |
8: |
4: |
9: Analog Gnd. |
5: Analog Output |
|
For use as a voltage output pins 1 and 6 are connected by a jumper.
For use as a monitor output the excitation voltage is fed into the reference input and the analog output is scaled down by a resistive divider.
Data Transmission across the RS 232 C Interface
The IAP-Monitor responds to single ASCII bytes:
To the monitor
´A´
´B´
´C´
Response
Mean pressure in ASCII string format, terminated by ´Carriage Return´.
Mean pressure in binary format, 1/10 mm Hg resolution, two´s complement, two
bytes, high byte first.
Instantaneous pressure in binary format, 1/10 mm Hg resolution, two´s complement,
two bytes, high byte first. Response only after new value is
read in (every 10 ms).
2
Contents
Safety instructions |
2 |
Indication and Method |
3 |
Monitor Operation |
4 |
Cleaning |
5 |
Connections |
6 |
Faults |
7 |
Technical Specifications |
8 |
Accessories |
10 |
Safety Instructions
The IAP-Monitor and the accom- |
Warning |
panying catheters are designed for |
The device is not intended |
the measurement of intraabdominal |
for use in areas where |
pressure. The manufacturer accepts |
there is a danger of |
responsibility for the safety, |
explosion. |
reliability and performance of the |
Warning |
monitor only if: |
|
|
The device may be |
- the installation, extensions, |
repaired only by persons |
readjustments, modifications and |
or companies that are |
repairs are performed by |
authorized to do so. |
authorized personnel, |
Warning |
|
|
- the electric installation of the |
The device is not intended |
room is in accordance with the |
for use during Electro- |
national regulations concerning |
Surgery/Diathermy. |
rooms used for medical |
Warning |
purposes, |
|
|
Grounding reliability can |
- the monitor is used in |
only be achieved if the |
accordance with the operating |
device is connected to an |
instructions, and |
equivalent power cord |
|
marked „hospital grade“ |
- the monitor is used with the |
or „hospital only“. |
approved accessories. |
|