Software
• Touch Screen inteface
• All Windows-R features available
• Reagents an patients identification entry bar code scanner
• 3 or 4 point standard curves for Ristocetin CoFactor assay
• CoFactor assay
• Eight digital timers, countdown, elapsed time, audible alarm
• On screen keyboard
• Data export to Prism 5, spreadsheet, templatem presentation
software and LIS (Laboratory Information System)
• Two level security and operator tracking
• Data analysis: User selectable point and functions, Primary
and secondary Slope, Area under the curve, Area under
the Slope, Lag phase, Shape change, Disaggregation
• Data sorting and Archiving
• Pre-loaded test parametrers
• User defined test protocols
• On screen help
• Online operator manual
• Diagnostics: Start-up, automatic and user selected
Accessories
Programmable pipettor
• Electronic with memory
• 10 to 300 uL capacity
• Multi-dispensing function
• Preprogrammed volumes
GraphPad-R Software Prism 5
• Bio-analytical software
• Templates for clinical, research, pharmaceutical, biotechnology
laboratories and contract research organizations.
Bar Code Scanner (optional)
• Bi-directional
• Supports 123 Scan setup utility
• RSS (Reduced Space Symbology)
• R
GTIN-Compliant
• Decode capability (16 Standard codes)
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PC specifications
• Dell Optiplex-TM
• Processor Pentium-R 3.2 GHz
• RAM 512 MB
• Hard disk 40 GB
• DVD/CD Read/Write 24X drive
• USB 2.0 (2) and RS232 (1) ports
• Network Ethernet
• Monitor ELO 1525L, Touch Screen, 15 inch, Flat LCD panel,
Active Matrix, Angolo 170°, 5-wire resistive
• Stendard keyboard, Touch Screen keyboard, Mouse
• Multifunction printer, color, inkjet
• Windows-R XP Professional Multi-Language Pack
Dimensions
• Typical configuration made of PAP-8E , PC e Monitor
• Height: 57,2 cm
• Width: 35,6 cm
• Length: 55,1 cm
• Weight: 21,0 Kg
Limited warranty
Two years parts and labor at the authorized distributor
Safety certifications
The PAP-8E analyser module meets:
European Union directive
98/79/EC invitro diagnostic medical devices,
European Union electromagnetic compatibility directive 89/336/EEC, European Union low voltage directive 73/23/EEC,
European standards:
EN 61010-1:2001,
Safety requirements for measurament control and laboratory use EN61010-2101:2002,
Particular requirements for invitro diagnostic (IVD) medical equipment,
EMC standards - EN 61326,
EN 61000-3-2; EN 61000-3-3.
The PAP-8E analyser is designed to agree
with the following standards: UL 61010-1 Safety requirements for electrical equipment for measurement, control and laboratory use - Part1: general requirements.
All accessory components have individual UL and CE certification.
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