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

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
About Thermo Fisher Scientific
Thermo Fisher Scientific’s mission is to enable customers to make the world healthier, cleaner and safer. Whether customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, they are there to support them. Thermo Scientific instruments, equipment, software, services and consumables address a range of needs from sample or material characterization and chemical analysis to clinical diagnoses and biological-based therapeutics manufacturing.
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