TECHNICAL SPECIFICATION
28
D-0115690-C (OM001)
– Otowave 102 Operating Manual
Languages
Operating Languages
English, German or French
Printing
Supported printer
Martel MCP8830 or Sanibel MPT-II
Interface
Infra-red, IrDA hardware, 9600 baud
Information printed
Tympanogram, Tympanogram analysis parameters,
Reflex graphs, Reflex analysis parameters, Serial
Number of device, Last and Next Due Calibration dates;
space for patient & clinician’s details to be entered.
Serial Interface to computer
Interface
OBEX (Object Exchange) service running on top of IrDA
stack. Auto-selects between 9600-115200 baud.
Information sent
Patient header, left and right ear data.
Power Supply
Battery Types
4 AA cells; either Alkaline (1.5V nominal) or NiMH
rechargeable (1.2V nominal, which must be 2.3 Ah
capacity or greater).
Warm-up period
None at room temperature
Number of recordings from one set of cells
Approx. 200 (Alkaline) or 100 (NiMH)
Auto power-off delay
90 or 180 seconds
Idle current
70mA
Current while testing
230mA
Physical
Display
128 x 64 pixels / 8 lines of 21 characters
Dimensions
190mm long x 80mm wide x 40mm high excluding probe
210mm long including probe
Weight (without batteries)
285 g
Weight (with batteries)
380 g
Environmental
Operating temperature range
+15
o
C to +35
o
C
Operating humidity range
30% to 90% RH, non-condensing
Operating atmospheric pressure range
980 to 1040 mb
Transport and storage temperature range
-20
o
C to +70
o
C
Transport and storage humidity range
10% to 90% RH, non-condensing
Transport and storage atmospheric pressure
range
900 to 1100 mb
Standards conformance
Safety
IEC 60601-1(plus UL, CSA & EN deviations)
EMC
IEC 60601-1-2
Performance
IEC 60645-5, Type 2 Tympanometer
CE mark
To the EU Medical Device Directive
15.2.
EQUIPMENT CLASSIFICATION
Type of protection against electric shock
Internally Powered
Degree of protection against electric shock
Type BF applied part
Degree of protection against ingress of water
Not protected
Mode of operation
Continuous operation
Equipment mobility
Portable
The Otowave 102 Tympanometer is classified as a Class IIa device under Annex IX of the EU Medical Devices
Directive.
Содержание Otowave 102
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