Why Choose a Medical Device Rated Blood Bank Refrigerator

Why does a blood bank refrigerator need to be certified as a Medical Device?

In the European Union, any equipment used for the storage of blood intended for transfusion must be classified and certified as a medical device, in accordance with the Medical Device Regulation (MDR 2017/745) or the previous Medical Device Directive (MDD 93/42/EEC). This legal requirement ensures that blood bank refrigerators meet strict standards for temperature control, safety, traceability, and performance—essential factors for patient safety and regulatory compliance.

Key Features and Benefits
- Validated temperature uniformity and stability across all storage levels
- Built-in alarm systems for deviations, door open, or power failure
- Temperature data logging with USB export and audit trail
- Access control for regulated usage
- Compliance with international guidelines

Why Fiocchetti Scientific?
Trusted across Europe and worldwide, Fiocchetti blood bank refrigerators combine Italian engineering with regulatory compliance, offering reliable performance in demanding clinical settings.
- Models available in various sizes to suit all storage needs
- Digital controllers with password protection
- Optional remote monitoring (CLOUD/GSM)
- Robust construction, energy-efficient operation, and easy maintenance
- Peace of Mind for Healthcare Providers
Whether you operate a healthcare facility, a private clinic, or a laboratory, storing blood safely and compliantly is non-negotiable. Using a medical device rated blood bank refrigerator ensures you meet health regulations while protecting the integrity of critical supplies.

Don’t compromise on storage when lives depend on precision. Choose Fiocchetti Scientific for certified performance, backed by expert technical support across Europe and worldwide.