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Desk Spirometers

Vitalograph ALPHA Spirometer (65002)

Product Code: 65002

£1347.54 ex. VAT
£1617.05 inc. VAT

Quantity:

65002 Vitalograph ALPHA Desktop Spirometer

The Vitalograph ALPHA™ is the spirometer of choice for respiratory care professionals around the world due to its ease of use, portability, integral printer and long term reliability.

The ALPHA features precise and durable measurement technology that requires no user calibration* and reduces costs by eliminating the need for expensive disposable sensors, turbines, spirettes or flow tubes. Optimal hygienic operation is assured via Vitalograph Bacterial Viral Filters (BVF™).

Features and Benefits

  • Measures VC, FVC, FEV1, FEV1 Ratio, PEF, FEF25-75% and more
  • On-screen visualisation of volume/time and flow/volume curves
  • Saves multiple pre-tests for subsequent post-testing
  • Compact Flash removable memory card slot
  • Presents the test information in clear, easy to read format
  • Links to PC via USB with Vitalograph Reports Software
  • Fast, silent printer that prints 140 tests per roll
  • Battery and mains power with integrated battery for off site testing
  • Real time clock
  • Autoclavable flowhead
  • Facility for user accuracy checks
  • Automatically selects the best test
 
Specification
 
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