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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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