Handheld transport monitor featuring ComfortCuff NIBP,
using measure-on-inflation technology.
Technical Specifications
Non-Invasive Blood Pressure
| Technique: |
Oscillometric measure upon inflation |
| Measurement Time: |
<40 sec, typical; 0 to 300mmHg; standard adult cuff |
| Automatic Measurement Cycles: |
5, 10, 15 min; Off |
| Inflation Pressure Range: |
0 to 300mmHg |
| Inflation Pressure, Max.: |
Adult: 300mmHg; Neonate: 150mmHg |
| Resolution: |
1mmHg |
| Accuracy: |
¡Ó2mmHg or ¡Ó2% of reading, whichever is greater, over full
range |
| STAT mode: |
5 min of continuous readings |
Heart (Pulse) Rate
| Range: |
30 to 300bpm |
| Accuracy: |
¡Ó2bpm or ¡Ó2%, whichever is greater |
| Update Time: |
Every measurement |
| Resolution: |
1bpm |
Displays
Type: LED
Parameters: Systolic; diastolic; heart rate
Status: Sensor: Low Battery; External Power; Neonatal Mode
Data Storage
Capacity: 100 measurements
System Output
Type: RS 232-compatible; digital; mini-din connector
Printer
Type: External thermal line printer; optional
Mechanical
Weight: With battery: 22.4 oz; 630g
Size: 7.5" (H) x 3.75" (W) x 1.75" (D); 19cm (H)
x 9.5cm (W) x 4.5cm (D)
Power Requirements
Voltage: 100 to 250 VAC; 50/60 Hz
Battery: Nickel metal hydride; life: 8 hr or up to 100 measurements,
typical; recharge time: 2.5 hr
Environmental
Operating Temperature: 32o to 113o F; 0o to 45o C
Storage Temperature: 23o to 131o F; -5o to 55o C
Operating Humidity: 15% to 90%, noncondensing
Classification
Type of Protection: Class II equipment
Degree of Protection: Type CF defibrillator-proof equipment
Safety: EN60601-1
Performance Standard: AAMI SP-10 1992
Approved by UL, CSA, CE.
Quality systems registered to ISO 9001 and CE marking per Annex
II, Clause 3 of Council Directive No. 93/42/EEC concerning medical
devices by TUV Product Service GmbH, Munich.
Specifications subject to change without notice.
Manufactured in USA.
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