CryoLyze
CRYO-LYO25
Laboratory freeze-drying / lyophilization technology designed to support controlled processing of sensitive biological, research and technical samples with preservation of sample quality.
Controlled Freeze-Drying for Sensitive Samples
CryoLyze is a laboratory freeze-drying / lyophilization technology developed for controlled processing of sensitive biological, research and technical samples. The system is intended to support preservation of sample quality and biological activity where relevant — depending on process validation.
The three-phase process — freezing, primary drying and secondary drying — is carried out under vacuum below approximately 3.5 kPa. Cooling is based on an LN2 concept. The AISI 316L chamber with clean laboratory surface finish is designed to support contamination-sensitive processing.
CryoLyze can be connected to the AeroVac Precision System (AVPS) for post-lyophilization clean handling, assembly and packaging — enabling a complete workflow from sample preparation to final packaging under controlled conditions.
Process Phases
NOTE: CryoLyze is a development platform. It is not presented as a medical device, GMP-certified system or pharmaceutical manufacturing equipment. Claims about sample preservation depend on process validation. Careful, process-specific validation is required for any regulated application.
CryoLyze — Technical Specifications
| Parameter | Target / Known Value | Note |
|---|---|---|
| System type | Laboratory freeze-drying / lyophilization technology | Development platform |
| Process phases | Freezing, primary drying, secondary drying | Configuration-dependent |
| Cooling concept | LN2-based concept | According to design |
| Vacuum target | Below approx. 3.5 kPa | Target / configuration-dependent |
| Chamber material | AISI 316L | Where applicable |
| Surface finish | Suitable for clean laboratory processing | Specification-dependent |
| Post-process handling | Possible AVPS connection | Optional workflow |
Parameters may vary depending on configuration and validation scope.
Discuss your sample type and process requirements
Discuss your sample type, process requirements and post-lyophilization handling workflow. We will help define a freeze-drying process configuration and assess possible integration with AVPS.