Industrial freeze-drying equipment & production lines

Equipment

Biomedical Freeze Dryers

HDF-FD01 to FD40 lyophilization families for biomedical research, diagnostics and regulated development.

Biomedical freeze dryers are lyophilization systems for research and development of biological and diagnostic materials — vaccines, biologics, plasma fractions and reagents. They are configured around the intended use, the container and the documentation the project requires, rather than sold as a one-size machine.

Who this is for

Best fitR&D laboratories, pilot teams and manufacturing groups developing a lyophilized biologic or diagnostic, or scaling a formulation before production.
Confirm firstProjects that already need a fully qualified production line should define their URS and regulatory market first, so the machine is specified to that requirement rather than retrofitted.

Where it is used

  • Formulation development — defining the freezing and drying curve for a new biologic.
  • Diagnostics and reagents — drying heat-sensitive materials to a stable powder.
  • Plasma and biological samples — laboratory-scale preservation with documented cycles.
  • Scale-up trials — carrying a bench recipe toward a production-sized dryer.

Model range and published parameters

The biomedical family spans HDF-FD01 to HDF-FD40. Reference values below are published for the silicone-oil heating configuration; the final unit is confirmed against the container, batch scale and documentation the project requires.

Model Drying area Footprint L×W×H Power Shelf Cold trap Vacuum Load Ice
HDF-FD01 1 m² 1600×1100×1800 mm 9 kW 4+1 -60 °C ≤5 Pa 10 kg 20 kg
HDF-FD02 2 m² 2800×1000×2500 mm 13 kW 5+1 -60 °C ≤5 Pa 20 kg 40 kg
HDF-FD03 3 m² 3200×1000×2500 mm 17 kW 6+1 -60 °C ≤5 Pa 30 kg 60 kg
HDF-FD05 5 m² 3500×1500×2500 mm 19 kW 5+1 -60 °C ≤5 Pa 50 kg 100 kg
HDF-FD10 10 m² 4500×1600×2500 mm 36 kW 8+1 -60 °C ≤5 Pa 100 kg 200 kg
HDF-FD20 20 m² 5800×1800×2800 mm 65 kW 12+1 -60 °C ≤5 Pa 200 kg 400 kg
HDF-FD30 30 m² 7800×2200×2800 mm 120 kW 11+1 -60 °C ≤5 Pa 300 kg 600 kg
HDF-FD40 40 m² 9800×2200×2800 mm 180 kW 15+1 -60 °C ≤5 Pa 400 kg 800 kg

Shelf temperature range is -45 to +70 °C across the family; heating is silicone-oil, cooling is air or water/air by scale. Published reference values from the HADOF biomedical catalog.

SUS304Chamber and shelf construction
-60 °CCold-trap temperature
≤5 PaWorking vacuum

How to choose a configuration

Research tier

For formulation and cycle development. A flexible control range and editable drying curve matter more than batch size.

Development tier

For a defined container and fill volume with batch records and reproducibility as the priority.

Customization scope

Shelf temperature range, condenser capacity, vacuum depth, stoppering or capping options, cleaning and sterilization features, and data-recording depth are configured per order. Intended use and regulatory market are confirmed up front because they determine documentation, not just hardware.

Quality control

URS reviewRequirements matched to the intended use before specification.
Component checkMaterials and purchased parts verified at incoming inspection.
Assembly testTemperature, vacuum and control loops validated in process.
RecordsTest data and documentation issued with the machine.
Pre-shipmentFinal inspection against the agreed configuration.

After-sales and documentation

Documentation scope — installation, operation, qualification support where applicable — is defined in the quotation. Remote support and spare-part guidance are available after delivery.

How pricing works

Price follows the configuration: scale, shelf and condenser duty, controls, cleaning or sterilization options, and the documentation package. A research-tier system costs less than a development-tier system with full records. Share the intended use and container and we quote the matching tier.

Frequently asked questions

Which model fits my material?

It depends on the container, batch size, target residual moisture and controls. Share your formulation and fill volume and we map it to a model.

Can you support qualification?

Documentation support is confirmed per project and market. Tell us the regulatory market and deliverables you need.

Do I need a stoppering option?

Only if you close vials inside the chamber under vacuum or controlled atmosphere; we confirm it against your closure system.

Share your URS and container →

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