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Panasonic MDF-382 Ultra Low Temperature Freezer

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Brand Panasonic
Origin Liaoning, China
Manufacturer Type Authorized Distributor
Product Category Domestic
Model MDF-382
Price Range USD 7,000–14,000
Instrument Type Horizontal
Effective Volume 330 L
Interior Dimensions (W×D×H) 490 × 600 × 1140 mm
Exterior Dimensions (W×D×H) 750 × 875 × 1850 mm
Power Supply 220 V, 50 Hz
Rated Power Consumption 680 W
Temperature Range −50 °C to −86 °C (1 °C increments
Compressor Dual-stage hermetic compressors (high-stage: 450 W
low-stage 750 W)
Refrigerant R404A
External Material Electrogalvanized steel with polyester powder coating
Internal Material Electrogalvanized steel with polyester powder coating
Doors 1 outer door, 2 inner doors
Safety Features High/low temperature alarm, power failure alarm, remote alarm contact, sensor self-diagnosis, compressor protection
Standard Accessories 1 set of keys, 3 stainless-steel shelves, 1 defrost scraper
Measurement Ports 3 × Φ17 mm (rear, lower-left, lower-right)

Overview

The Panasonic MDF-382 Ultra Low Temperature Freezer is a horizontally configured, high-reliability cryogenic storage system engineered for long-term preservation of biological samples—including primary cells, stem cell lines, genomic DNA, RNA, proteins, and archived clinical specimens—at sustained temperatures ranging from −50 °C to −86 °C. Its dual-stage cascade refrigeration architecture employs two independent hermetic compressors (450 W high-stage, 750 W low-stage) and environmentally compliant R404A refrigerant to achieve thermodynamic stability under variable ambient conditions (10–30 °C). The unit’s vacuum-insulated cabinet—constructed from electrogalvanized steel with durable polyester powder coating—minimizes thermal bridging and reduces heat ingress, enabling consistent temperature uniformity across the 330 L effective storage volume. Designed for integration into regulated laboratory environments, the MDF-382 meets core engineering requirements for ISO 13485-aligned biobanking workflows and supports GLP-compliant sample integrity protocols.

Key Features

  • Dual-stage cascade refrigeration system delivering stable operation at −86 °C without liquid nitrogen dependency
  • Microprocessor-controlled temperature monitoring with ±1 °C accuracy and 1 °C adjustable setpoint resolution
  • Front-accessible condenser filter with automatic clogging detection and visual status indicator
  • Ergonomic single-hand external door handle with optional padlock-compatible locking mechanism for access control
  • Three standardized Φ17 mm measurement ports (rear, lower-left, lower-right) for real-time temperature probe insertion or data logger integration
  • Comprehensive safety suite: independent high/low temperature alarms, power failure alert with battery-backed memory, remote alarm relay output (dry contact), sensor fault auto-diagnosis, and compressor overheat/overload protection
  • Compact footprint (750 × 875 × 1850 mm) optimized for placement within standard laboratory rooms or cleanroom antechambers

Sample Compatibility & Compliance

The MDF-382 accommodates standard cryovial racks (2 mL, 5 mL), Nunc™ CryoBoxes®, and 100 mm Petri dish stacks within its 490 × 600 × 1140 mm interior cavity. Its validated temperature stability supports storage of materials governed by USP , ISO 20387:2018 (biobanking), and ICH M10 (bioanalytical method validation) requirements. While not certified to FDA 21 CFR Part 11 out-of-the-box, the freezer’s alarm logging and event timestamping capabilities—when paired with validated third-party environmental monitoring software—enable audit-ready documentation for GxP environments. All structural materials comply with RoHS Directive 2011/65/EU and are non-outgassing under continuous cryogenic exposure.

Software & Data Management

The MDF-382 operates via an embedded microcontroller with non-volatile memory that retains alarm history and operational events during power interruption. It does not include built-in Ethernet or USB connectivity; however, its dry-contact remote alarm output and analog temperature signal (0–5 V or 4–20 mA optional via external module) allow seamless integration with centralized lab infrastructure systems such as Siemens Desigo CC, Honeywell Experion PKS, or LabVantage LIMS. Users may configure alarm thresholds, enable/disable audible alerts, and review recent temperature excursions directly on the front-panel LCD interface. For regulatory traceability, periodic manual export of log data via RS-232 (optional adapter) is supported—consistent with ISO/IEC 17025 clause 7.7.1 for equipment calibration and performance verification records.

Applications

  • Long-term archival storage of human tissue specimens and PBMCs in clinical biobanks
  • Cryopreservation of induced pluripotent stem cell (iPSC) master cell banks under cGMP Annex 1 guidelines
  • Stabilization of thermolabile enzymes and monoclonal antibody drug substances prior to analytical characterization
  • Backup cold storage for −80 °C dependent assays including qPCR template preparation and ELISA plate pre-chilling
  • Supporting ISO 15189-accredited medical laboratories requiring documented cold chain continuity for diagnostic sample retention

FAQ

What is the minimum ambient temperature required for stable −86 °C operation?
The MDF-382 is rated for uninterrupted performance at −86 °C when installed in environments maintained between 10 °C and 30 °C. Operation below 10 °C may reduce compressor efficiency; above 30 °C requires additional ventilation clearance per Panasonic Technical Bulletin TB-MDF-382-02.

Can the unit be validated for IQ/OQ/PQ in a pharmaceutical quality system?
Yes—the MDF-382’s mechanical design, alarm architecture, and temperature repeatability support qualification per ASTM F2697-22 and EU GMP Annex 15. Full validation packages require third-party thermocouple mapping and alarm response testing; Panasonic provides factory calibration certificates traceable to NIST standards.

Is R404A refrigerant compliant with current F-Gas Regulation (EU) No 517/2014?
R404A has a GWP of 3922 and is subject to phase-down quotas under EU F-Gas Regulation. While permitted for servicing existing equipment, new installations in the EEA must comply with Article 11 restrictions. Customers in regulated markets should consult local HVAC contractors regarding future retrofit pathways to lower-GWP alternatives.

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