Vitalograph ALPHA
Vitalograph · Model ALPHA
Integral thermal printer Durable measurement technology without the need for expensive disposable sensors, turbines, spirettes or flow tubes Optimal hygiene via Vitalograph Bacterial Viral Filters (BVF) No user calibration required* Simple and intuitive navigation Built-in interpretation of measurement results Mains or battery powered Includes all parameters for adult and pediatric patients within general healthcare and occupational health Includes Vitalograph Reports Software with the ability to create editable PDFs Features latest GLI spirometry predicted equations and Z-scores
Key tips
- ·When no category-specific guidance fits, default to the manufacturer's own service manual and the general troubleshooting method in the Engineer's Guide.
- ·Run an incoming and annual electrical safety test regardless of how niche the device is.
PM Checklist
Preventive-maintenance tasks typical of this equipment class. Perform to the manufacturer's procedure and your facility's policy - this is general reference, not a schedule for this specific unit.
- ·Follow the manufacturer's PM schedule
- ·Perform incoming and annual electrical safety testing per facility biomedical program
Technical Specs
- Product
- Vitalograph ALPHA
- Model Number
- 6000
- Size
- 300 x 250 x 75mm
- Weight
- 2kg net
- Parameters
- Varies by country variant
- Operating Temperature Range
- ATS Limits: 17-37°C Design Limits: 10 - 40°C
- Voltage/Frequency
- 110 - 250V~50/60Hz
- Flow Detection Principle
- Fleisch type pneumotachograph
- Volume Detection
- Flow Integration sampling @ 100Hz
- Accuracy when in Operating Range
- Flow +/- from 10% to 5% Max flow rate +/-16L/s Min flow rate +/-0.02L/s
- Volume Accuracy
- Better than +/-3%
- Maximum Displayed Volume
- 10L
- Maximum Test Duration
- 90 seconds
- Flow Impedance
- 0.1kpa L/s @ 14L/s Complies with ATS/ERS 2005
- Printer
- Thermal
- Performance Standards
- ATS/ERS 2005 ISO 26782:2009 ISO 23747:2007
- Safety Standards
- IEC 60601-1:2005
- Medical Safety Standard
- Medical Devices Directive 93/42/EEC as amended
- Designed & Manufactured Under
- ISO 13485:2003 and 2016 FDA 21 CFR 820 CMDR
- Communications
- USB and Compact Flash
Typical Location
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
- Varies by device - check the unit's own manual for facility placement guidance
Documents & Manuals
Troubleshoot this device with Bio
Describe a symptom or error code. Bio answers from this device's own documented error codes, failure modes, parts, and guides.
Ask Bio →