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TW 3000 Multichamber

Multi-Chamber Washer Disinfector

The TW 3000 is a fully automatic multi-chamber tunnel washing system, ideal for facilities processing large volumes of medical devices. Independent chambers allow for simultaneous cycles, increasing productivity. Its modular design allows for configurations of 3 to 5 chambers, customizable for pre-wash, ultrasonic, washing, rinsing, thermal disinfection, and drying, based on specific operational needs.
High productivity requires the use of fixed automatic loading/unloading systems or ATS and M-ATS shuttles.

Robotic Kits

MIS Instruments

Ophthalmic Instruments

Anaesthesia Instruments

Orthopaedic Instruments

Bulky Items

Features

Modularity

The system can be configured from 3 up to 5 chambers, depending on throughput requirements.

Inspection Windows

Every module is equipped with a dedicated fully-sealed inspection window for easy maintenance and routine cleaning operations.

Ultrasonic Treatment

TW 3000 Multichamber Series can be equipped with an ultrasonic module for the automatic treatment of the loads. It is also possible to skip the passage through the module when not needed.

Drying Efficacy

An efficient system – carefully and evenly distributing air on all chamber zones and washing rack levels – ensures perfect drying of all instruments and tubes with HEPA H14 filtered air injection.

Configurations

TW 3000/3

Overall Dimensions WxDxH
2100 x 2397 x 2650 mm

Chamber Volume
~500 lt / 17.66 cu ft

Wash Cart Volume
~350 lt / 12.36 cu ft

Load Capacity
Up to 18 DIN 1/1 trays per chamber

TW 3000/4

Overall Dimensions WxDxH
2100 x 3942 x 2650 mm

Chamber Volume
~500 lt / 17.66 cu ft

Wash Cart Volume
~350 lt / 12.36 cu ft

Load Capacity
Up to 18 DIN 1/1 trays per chamber

TW 3000/5

Overall Dimensions WxDxH
2100 x 4854 x 2650 mm

Chamber Volume
~500 lt / 17.66 cu ft

Wash Cart Volume
~350 lt / 12.36 cu ft

Load Capacity
Up to 18 DIN 1/1 trays per chamber

Steelco-branded washer disinfectors are designed to comply with the European EN ISO 15883-1/2/5 guidelines on performance, EN ISO 14971, EN 61010-1/2-040, EN IEC 61326-1, EN 62366 guidelines on safety, and EN 62304 guidelines on software design. They are classified CE0051 legacy medical devices (Directive 93/42/EEC, MDD).