Oral-Fluid Drug Testing System 5000 (Non-IVD)

The Oral-Fluid Drug Testing System 5000 (Non-IVD) is a fast, accurate analyser-based system for testing oral fluid samples for drugs of abuse, supplied for law enforcement use only.

Key features

• Tests oral fluid samples for amphetamines, designer amphetamines, opiates, cocaine and metabolites, benzodiazepines, cannabinoids and methadone.
• Easy data management through the dedicated diagnostics software.
• Test kits available for 5, 6, 7 or 8 substances (cocaine, opiates, benzodiazepines, cannabis, amphetamine, methamphetamines, methadone and ketamine, depending on the kit).
• Typical measurement time under 9 minutes, depending on the test kit used.
• Optional analysis in under 5 minutes by increasing the THC cut-off to 25 ng/ml (after updating the device software).
• Stores 500 records or measurements.
• Training test kits available (3 positive, 3 negative per set of 6).
• Optional accessories: compact keyboards (German QWERTZ, English QWERTY, French AZERTY), barcode reader, mobile printer, carrying case and hard shell carrying case.
• Supplied with power supply and 12 V car cable.

Technical data

• Operating voltage: 12 V direct voltage (via supplied power pack)
• Power input: normally 3 A
• Dimensions (W x H x D): 200 x 260 x 250 mm
• Weight: 4.5 kg
• Operating temperature: 4 °C to 40 °C
• Storage / transportation temperature: -20 °C to +60 °C
• Relative humidity: 5 to 95 % (non-condensing)
• Ports: optical for printer, PS/2, USB Slave
• Time of measurement: depending on the test kit used (typically < 9 minutes); optional analysis in < 5 minutes by increasing the THC cut-off to 25 ng/ml (after updating the device software)
• Storage capacity: 500 records or measurements
• Licences / standards: Licensed as a medical product within the EU in accordance with Directive 98/79/EC on in vitro diagnostic medical devices (IVD). Outside the European Union for non-medical use (Standard) or for forensic use (UKCA-conform). This Non-IVD version is the Standard variant.
• Test method: Qualitative detection of target substances or their metabolites in a sample above a specified threshold concentration (cut-off), providing a preliminary analytical result (screening procedure). The detectable substances are defined by the specific test kit used.
• Confirmation: A more specific method must be applied to obtain a confirmed result; the preferred method is generally gas chromatography/mass spectrometry (GC/MS). Professional evaluation of results must consider the broader clinical context of the individual tested, particularly for a preliminary positive result.

Supplied, installed, trained and serviced across India by Dawell Lifescience, with calibration and AMC support.