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Applied Biosystems VeritiPro Dx: IVDR-Compliant, CE-IVD Labeled Diagnostic Thermal Cycler

The Applied Biosystems VeritiPro Dx Thermal Cycler is an in vitro diagnostic (IVD) endpoint thermal cycler designed to amplify nucleic acids from human-derived specimens using polymerase chain reaction (PCR). It is manufactured to ISO 13485 and GMP requirements.

VeritiPro Dx Thermal Cycler conforms to:
- EU 2017/746 requirements and is CE- IVD labeled in Europe
- Classified as US-FDA class I medical device
- UK Medical devices regulations 2002 and is UKCA labeled in UK

This instrument delivers precise temperature control with a ramp rate of 6.0°C/sec. There is no need for protocol re-optimization when upgrading from Veriti Dx Thermal Cycler; the simulation mode supports seamless transition


Product Specifications
Block format 96-well, 0.2mL alloy block
Maximum block ramp rate 6.0°C/sec
Temperature accuracy ±0.25°C (35–99.9°C)
Temperature range 0–100°C
Reaction volume range 10–100 µL
VeriFlex Blocks range 6 temperature zones; supports 25°C across block (5°C zone-to-zone)
Number of programs Up to 1,000 protocols
VeritiPro Dx dimensions (L x W x H) 46.5 x 24.5 x 21.7 cm (18.3 x 9.7 x 8.5 in.)
Weight 12 kg (26.5 lb)
Voltage 100–120 V; 200–240 V, 50/60 Hz
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