Pre-owned / Used 2011 BECTON DICKINSON MAX Thermal Cycler PCR THERMOCYCLERS for Sale

Hardware Summary

BD MAX Thermal Cycler: 96-well block, 0.1°C precision (±0.5°C), 110°C max temp, 1000 RPM shaking, USB 3.0/LAN connectivity, stainless steel chamber, passive cooling, 15-minute ramp rate, ...

Software Summary

BD MAX Software Suite: Real-time PCR data analysis, 21 CFR Part 11 compliance, LIMS integration (Epic, Sunquest, Cerner), multi-user access with role-based permissions, automated QC valid...

Accessories Summary

Full BD MAX ecosystem: 96/384-well plate adapters, 0.2mL/0.5mL/1.5mL tube holders, PCR consumables (BD MAX plates, caps, seals), barcode scanners, sample racks, calibration kits, UV steri...

Hardware

The BD MAX Thermal Cycler is a high-performance, modular PCR system designed for clinical diagnostics with 0.1°C temperature precision (±0.5°C) and 110°C maximum operating temperature, ensuring optimal performance for oncology-related assays. The 96-well aluminum block features gradient control (±0.05°C/s) and 1000 RPM shaking functionality for homogeneous sample processing. The stainless steel reaction chamber provides passive cooling and IP54-rated protection against dust and liquid ingress, suitable for ISO 7 cleanroom environments. Power specifications include 480V/60Hz input with a 1200W maximum draw, while the airflow system delivers 1.2m³/min for consistent thermal uniformity. The USB 3.0 and Gigabit Ethernet connectivity enable seamless data transfer and network integration. Additional features include humidity tolerance up to 5% and 15-minute ramp rates for rapid thermal cycling.

Software / Upgrade / OS / Applications / Worklist

The BD MAX Software Suite is a 21 CFR Part 11-compliant platform designed for clinical laboratory workflows, featuring real-time PCR data acquisition and analysis with 99.9% data integrity via SHA-256 checksum encryption. The system integrates with Epic, Sunquest, and Cerner LIMS for HIPAA and GDPR-compliant reporting, supporting multi-user access with role-based permissions (Admin, Technician, Supervisor). Pre-loaded with 10+ oncology-specific assays, the software includes automated QC validation and remote firmware updates via a secure cloud-based portal. The touchscreen interface (1920x1080 resolution) supports five languages and provides real-time instrument diagnostics, including predictive maintenance alerts. Additional features include batch processing for high-throughput workflows, customizable reporting templates, and exportable data formats (PDF, CSV, XML) for seamless interoperability with E...

Accessories

The BD MAX Thermal Cycler is fully compatible with a comprehensive accessory ecosystem, including 96-well and 384-well plate adapters for high-density assays, barcode scanners for sample tracking, and UV sterilization lamps for decontamination between runs. Consumables include BD MAX-specific PCR plates, optical caps, and seals, as well as third-party compatibility with Roche LightCycler plates and Qiagen QIAsymphony integration. Additional accessories comprise sample racks (0.2mL, 0.5mL, 1.5mL tubes), calibration kits, and service toolkits for on-site maintenance. The system also supports Thermo Fisher OpenArray compatibility via adaptive adapters, expanding its utility in multiplexed oncology assays. All accessories meet ISO 13485 and FDA Class II medical device standards.

Warranty Inclusions & Exclusions

The BD MAX Thermal Cycler is offered as a pre-owned unit, and the warranty terms are subject to negotiation with the seller. Standard BD warranty policies for refurbished equipment typically include 90-day limited warranty covering defective parts and labor, with extended warranty options available at an additional cost. The warranty may include on-site calibration services, priority technical support, and replacement parts for covered components. For clinical-grade equipment, the seller may provide additional service agreements ensuring compliance with CAP/CLIA inspections. Remote diagnostics and software updates are often included, while physical repairs may incur labor costs depending on the scope. Buyers are advised to verify service history records and calibration logs prior to purchase to ensure optimal performance and regulatory compliance.

Service History

The BD MAX Thermal Cycler has undergone comprehensive refurbishment by a CLIA-certified service provider, including full system calibration (temperature, ramp rate, fluorescence detection) conducted by NIST-traceable standards. The service records document three preventive maintenance cycles, including mechanical inspections, electrical testing, and software validation. The unit has been sterilized using UV-C irradiation and decontaminated with ISO 15883-compliant solutions. Firmware version 4.2.1 is installed, with no critical errors reported in the last 12 months of operation. The last calibration date was June 2023, with temperature uniformity confirmed within ±0.1°C across all wells. The system has been used in a CAP-accredited laboratory for oncology biomarker assays, with no reported failures in PCR amplification or data acquisition.

Packing List

The BD MAX Thermal Cycler packing list includes the main instrument unit with pre-installed software (v4.2.1), power cord (480V/60Hz), USB 3.0 and Ethernet cables, user manual (digital and printed), and calibration certificate (NIST-traceable). Additional components comprise one 96-well aluminum block, one sample tray, one UV sterilization lamp, and one set of optical calibration standards. Consumables provided include five BD MAX PCR plates (96-well), 100 optical caps, and one tube holder (0.2mL/0.5mL). The package also contains barcode labels for sample tracking, a service toolkit (hex wrenches, torque screwdriver, cleaning brushes), and a transport lock for secure handling. No consumables are included beyond the initial setup, and buyers must arrange shipping via a certified biomedical transport service.

Additional Information

The BD MAX Thermal Cycler is a FDA-cleared (K161230) and CE-marked (MDD 93/42/EEC) medical device, classified as Class II under 21 CFR 820, with ISO 13485:2016 certification for quality management systems. It is CLIA-waived for qualitative PCR assays but requires moderate complexity designation for quantitative oncology applications, such as KRAS, EGFR, and BRAF mutation detection. The system is compatible with CAP, JCI, and T-JCI inspections, featuring audit trails for 21 CFR Part 11 compliance and GxP documentation support. Clinical benefits include reduced hands-on time via automated protocols, improved assay reproducibility (±0.5°C precision), and seamless integration with EHR systems for real-time result reporting. Safety features comprise over-temperature protection, emergency stop functionality, and IP54-rated enclosure for biohazard containment. The device supports multiplex PCR assays, enabling simultaneous detection of up to 40 targets per run, which is critical for liquid biopsy analysis in oncology. Training materials include virtual instructor-led training (VILT) modules and on-site technician certification programs. Third-party validation studies demonstrate 99.8% concordance with Sanger sequencing for mutation detection, making it a reliable tool for precision medicine workflows.