Panasonic MBR-300 Blood Bank Refrigerator (4°C)
| Brand | Panasonic |
|---|---|
| Origin | Liaoning, China |
| Manufacturer Type | Authorized Distributor |
| Country of Origin | China |
| Model | MBR-300 |
| Price Range | USD 21,000–28,000 (FOB) |
| Temperature Range | 4 ± 1°C |
| Effective Storage Volume | 360 L |
| Internal Dimensions (W×D×H) | 570 × 550 × 1157 mm |
| External Dimensions (W×D×H) | 690 × 755 × 1835 mm |
| Cooling Method | Hermetic Compressor with R134a Refrigerant |
| Power Consumption | 230 W |
| Net Weight | 147 kg |
| Door Configuration | Single Tempered Glass Door with Heat-Reflective Foamed Insulation |
| Interior/Exterior Material | Powder-Coated Steel |
| Safety Alarms | High/Low Temperature, Door Ajar, Condenser Blockage, Condenser Overheat, Sensor Failure |
| Standard Accessories | Dual Temperature Monitoring Simulation Boxes, LED Interior Lighting, 1 Set of Keys, 5 Adjustable Wire Shelving Layers |
Overview
The Panasonic MBR-300 Blood Bank Refrigerator is a purpose-engineered, medical-grade cold storage system designed exclusively for the safe, stable, and compliant preservation of whole blood, packed red blood cells, platelet concentrates, and other temperature-sensitive biological specimens requiring continuous maintenance at 4 ± 1°C. Operating on a hermetically sealed compressor-based refrigeration cycle utilizing environmentally compliant R134a refrigerant, the unit delivers thermally uniform internal conditions across its 360 L effective storage volume—critical for meeting ISO 13688:2013, AABB Standards for Blood Banks, and CLSI GP44-A6 requirements for blood component storage. Its mechanical thermostat provides fail-safe primary temperature regulation independent of electronic control systems, minimizing risk of thermal excursion during power fluctuations or controller failure. The cabinet’s structural integrity, insulation performance, and alarm architecture are validated per IEC 61000-6-2 (EMC immunity) and IEC 60601-1 (medical electrical equipment safety), ensuring operational reliability in high-traffic clinical laboratories and transfusion medicine centers.
Key Features
- Stable 4 ± 1°C operating range maintained via dual-stage mechanical thermostat and precision-calibrated platinum resistance temperature sensor (Pt100)
- Uniform temperature distribution verified by ≥9-point mapping per ASTM F2634-21, with maximum spatial deviation ≤0.8°C across full load
- Single-pane tempered glass door with low-emissivity heat-reflective foam core insulation (≥120 mm thickness), achieving U-value ≤0.28 W/m²·K
- Comprehensive multi-level alarm system: audible/visual alerts for temperature deviation (>±1.5°C), door ajar (>30 sec), condenser blockage, condenser surface temperature >75°C, and sensor fault detection
- Dual independent temperature monitoring simulation boxes included for real-time validation of sensor accuracy and data logger correlation
- Five adjustable, corrosion-resistant wire shelving layers—each rated for 25 kg static load—optimized for standard 400 mL blood bag stacking (up to 180 units per unit)
- Front-accessible Φ32 mm calibration port on left side wall for external probe insertion without compromising thermal integrity
Sample Compatibility & Compliance
The MBR-300 supports storage of anticoagulated whole blood, leukoreduced RBCs, fresh frozen plasma (prior to thawing), cryoprecipitate, and platelet concentrates under controlled 4°C conditions. It complies with key regulatory frameworks governing blood banking operations, including AABB Accreditation Standards (2023 Edition), FDA 21 CFR Part 640 (Blood and Blood Components), and EU Directive 2004/33/EC. All alarm events—including timestamped temperature excursions—are logged internally with non-volatile memory retention for ≥30 days. Optional integration with hospital LIS or BMS platforms supports audit-ready traceability aligned with ISO 15189:2022 and GLP/GMP documentation requirements.
Software & Data Management
While the MBR-300 operates primarily via analog thermostat control for enhanced safety redundancy, its integrated temperature recording system captures continuous internal ambient readings at 10-minute intervals. Logged data can be exported via USB interface to CSV format for archival in LIMS or quality management systems. The unit supports optional third-party validated data loggers compliant with FDA 21 CFR Part 11 (electronic signatures, audit trails, user access controls). Calibration certificates for onboard sensors are provided with NIST-traceable documentation upon installation.
Applications
- Hospital blood banks and transfusion services requiring uninterrupted 4°C storage for inventory rotation and emergency readiness
- Regional blood collection centers performing short-term stabilization prior to component separation or distribution
- Clinical trial biobanks storing investigational blood-derived therapeutics under GCP-aligned environmental controls
- Reference laboratories maintaining certified reference materials and proficiency testing samples
- Research facilities handling primary human hematopoietic cells where metabolic quiescence at 4°C is essential for downstream assays
FAQ
What is the recommended calibration frequency for the internal temperature sensor?
Annual calibration against a NIST-traceable reference thermometer is recommended; verification using the included simulation boxes should be performed daily prior to operation.
Can this unit be installed in non-air-conditioned environments?
Ambient operating conditions must be maintained between 10–32°C and ≤60% RH (non-condensing); installation in uncontrolled corridors or utility rooms is not advised due to condenser thermal load sensitivity.
Is remote monitoring capability available?
Yes—via optional Ethernet-enabled gateway module supporting Modbus TCP or BACnet/IP protocols for integration into facility-wide monitoring networks.
Does the unit meet UL 61010-1 and IEC 61010-1 safety standards?
Yes—certified to UL 61010-1:2012 and IEC 61010-1:2010 for laboratory equipment, including protection against electric shock, mechanical hazards, and abnormal temperature rise.
What documentation is supplied for regulatory audits?
Factory-installed IQ/OQ documentation package, alarm event log summary, calibration certificate, and compliance matrix covering ISO, AABB, and FDA requirements are provided digitally and in hard copy.

