cGMP decontamination DPB
PHARMA DIVISION
cGMP decontamination DPB description
The DPB equipment has been designed to decontaminate thermolable materials, such as plastic syringe trays, electronic components, pre-sterilised material, disinfectants, etc.
SOLIDS AND SEMI-SOLIDS
AIR + HYDROGEN PEROXIDE
20°C – 30°C
Process Features
Predefined and “custom” programmes for every need. The equipment process is developed by our Automation Department, according to the current regulations/standards and the type of product being decontaminated. A product that must be moved from a dirty environment to a clean one, and vice versa, by means of a hydrogen peroxide (H2O2) decontamination cycle. The process has been developed to ensure a homogeneous gas distribution and reduced throughput times.
Additional Information
- Square or rectangular washing chamber and hatches (doors).
- AISI 316 L chamber and doors.
- All the edges are rounded to ensure optimum surface hygiene.
- The “U”-shaped reinforcements welded on the outside of the chamber ensure its stability.
- The internal ventilation system ensures that the hydrogen peroxide is optimally distributed on the load.
- Catalytic chamber degassing system.
- The pass box chamber is positioned on a tubular-type base to evenly distribute the weight on the floor.
- The loading trolley-inserting and removing guides are positioned on the bottom of the chamber. These guides are also height-adjustable.
- Two 1.5” tri-clamp ferrules are welded to the chamber for validation purposes.
- All of the chambers internal surfaces are mechanically polished and then subjected to chemical degreasing, pickling and passivation treatments. Surface finish: ≤ 0.35 micron.
- Above-floor or recessed chamber installation possible for large volumes.
- The unloading door has been designed to be connected to the walls of the clean chambers (“Bio-seal” interface).
