Operating Room Control Panel
| Applications | For Operating Rooms |
| Other Characteristics | With Touchscreen |
| Applications | Medical, Laboratory, For The Pharmaceutical Industry |
| Configuration | Floor-Standing |
| Function | Automatic |
| Sterilization Chamber Material | Stainless Steel |
Associated tags
Product review
Catalog record
Inquiry support
Product summary
The primary distinction between the Ventilab® PL and the Vakulab® PL is the taller chamber, which enables the installation of a fan without compromising the chamber volume. Furthermore, the "Closed solutions" software package, chamber wall, temperature probe, and fan are all included as standard features for sterilizing liquids in closed containers.input:
output:The expert in the field of steam/air mixture processes.input:
output:The Vakulab® PL is the optimal choice for the sterilization of solid and porous materials, liquids in open or loosely sealed containers, and infectious waste and liquids in closed containers through the steam/air mixture process.input:
output:The sterilizer is CE-marked in accordance with the Pressure Equipment Directive (PED) 2014/68/EU and the Machinery Directive 2006/42/EC. The standards that are implemented are DIN 58951-2. AD 2000 Design of Pressure Vessels, DIN EN 62304, and steam sterilizers for laboratory use Software for medical devices. The internal walls of the sterilization pressure vessel are constructed from stainless steel, with a material number of 1.4404 (AISI 316 L) and the steam jacket is made from 1.4571 (AISI 316 Ti). The vessel is double-walled. Steam-conducting pipes and valves are manufactured from stainless steel, and the piping system is designed in accordance with DIN EN 285. The pipes are thermally insulated and color-coded. In accordance with DIN EN 62304, software validation, and DIN EN 285 for electrical equipment for measurement and control.input:
output:B&R controllerinput:
output:A ten-inch displayinput:
output:Active jacket coolinginput:
output:Cooling circuit connection and recirculation coolingISA is an acronym for Intelligent Service Advisor.input:
output:Special RKI waste programinput:
output:Filtration of exhaust airInactivation of condensate
output:The expert in the field of steam/air mixture processes.input:
output:The Vakulab® PL is the optimal choice for the sterilization of solid and porous materials, liquids in open or loosely sealed containers, and infectious waste and liquids in closed containers through the steam/air mixture process.input:
output:The sterilizer is CE-marked in accordance with the Pressure Equipment Directive (PED) 2014/68/EU and the Machinery Directive 2006/42/EC. The standards that are implemented are DIN 58951-2. AD 2000 Design of Pressure Vessels, DIN EN 62304, and steam sterilizers for laboratory use Software for medical devices. The internal walls of the sterilization pressure vessel are constructed from stainless steel, with a material number of 1.4404 (AISI 316 L) and the steam jacket is made from 1.4571 (AISI 316 Ti). The vessel is double-walled. Steam-conducting pipes and valves are manufactured from stainless steel, and the piping system is designed in accordance with DIN EN 285. The pipes are thermally insulated and color-coded. In accordance with DIN EN 62304, software validation, and DIN EN 285 for electrical equipment for measurement and control.input:
output:B&R controllerinput:
output:A ten-inch displayinput:
output:Active jacket coolinginput:
output:Cooling circuit connection and recirculation coolingISA is an acronym for Intelligent Service Advisor.input:
output:Special RKI waste programinput:
output:Filtration of exhaust airInactivation of condensate
Shipping & Delivery FAQ
How are products prepared before shipment?
Each item is checked against the catalog record, protected with suitable packaging materials, and prepared with available product documentation for procurement review.
Can you support international delivery requests?
The support team can coordinate delivery options by destination, product type, and documentation requirements before confirming availability.
Are fragile or calibrated products handled differently?
Sensitive products are packed with additional cushioning and handling notes; calibration or compliance documents can be reviewed during the inquiry process.
How can I estimate lead time?
Lead time depends on stock status, destination, carrier availability, and any requested documentation. Contact the product team for a product-specific estimate.
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