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SPE Series

Closure processing system

Processes container closures — vial stoppers and caps, syringe plungers and needle shields, cartridge lined seals — combining washing, siliconization, sterilization and drying in one GMP solution. A wide range of closure transfer methods are available to reduce risk of contamination associated with manipulations. Automated line clearance and closure counting support batch integrity and faster changeovers. More than 200 systems are installed worldwide.

Typical loads
Suitable for processing a wide range of container closures, including:

  • Vial stoppers and caps
  • Syringe plungers and needle shields
  • Cartridge plungers and lined seals

Features

Sanitary GMP construction

Built for sanitary application in regulated environments: fully drainable designs, non-retentive surfaces and 316L stainless steel with a smooth finish. Welds are ground flush and fabrication can be documented in a complete logbook. Process-contact materials with EN 10204 traceability and USP Class VI compliant elastomers.

Site-specific layout, including multi-level

Multiple discharge options support site-specific layouts, including configurations adapted to different room constraints and workflow requirements. Systems can be integrated into multi-level installations with separate process and machinery floors, helping optimize space utilization and maintain clear separation between operational and technical areas.

Cycle development and validation support

We develop cycles around your loads and acceptance criteria, then document them in a qualification package aligned to your project scope. Risk-based cycle definition, mapping and test support help you reach a robust, repeatable process sooner.

Remote diagnostics and support

A secure, on-demand remote gateway provides controlled diagnostic access for your maintenance team and SteelcoBelimed support when authorized. Faster troubleshooting can reduce downtime while meeting industrial cybersecurity requirements.

SteelcoBelimed equipment for pharmaceutical applications is designed and manufactured in accordance with cGMP principles and within an ISO 9001–certified quality system. All systems are developed to meet applicable international pharmaceutical regulations (FDA, EU GMP), as well as relevant electrical, EMC and safety requirements.

Five standard capacities: 40 to 240 L / 1.4 to 8.4 cu ft

Model Useful volume Volume per basket  Number of baskets
SPE-40 40 Lt / 1.4 cu ft 10 Lt / 0.35 cu ft 4
SPE-80 80 Lt / 2.8 cu ft 10 Lt / 0.35 cu ft 8
SPE-120 120 Lt / 4.2 cu ft 10 Lt / 0.35 cu ft 12
SPE-180 180 Lt / 6.4 cu ft 10 Lt / 0.35 cu ft 18
SPE-240 240 Lt / 8.5 cu ft 12 Lt / 0.42 cu ft 20