Operating Room Control Panel
| Applications | For Operating Rooms |
| Other Characteristics | With Touchscreen |
| Applications | Containment, Sterile, For The Pharmaceutical Industry |
| Other Characteristics | Glove Box, Positive Pressure, Flexible |
| Class | Class Iii |
| Configuration | Floor-Standing |
Associated tags
Product review
Catalog record
Inquiry support
Product summary
Sterisafe® isolators are intended for sterile preparations and handling.input:
output:Sterisafe® isolators guarantee personnel protection and containment. The "moving forward" principle is upheld, and each production operation (including the output of finished products, the removal of waste and remainders, and the management of remainders) adheres to a designated circuit to mitigate the risk of cross-contamination.input:
output:The HEPA filtered air flow (turbulent, unidirectional, or laminar) and the pressure mode are customized to your specific application in accordance with the recommendations and standards for isolation technology in healthcare institutions.input:
output:Sterisafe® isolators have been developed in close collaboration with our end users. Work ergonomics are optimized with a variety of standard comfort features.
input:
output:Our designers are delighted to assist you in the customization and configuration of your equipment to meet your requirements.input:
output:Modular design: Two gloves or two pairs of gloves in a line or face-to-faceinput:
output:Structure that is either flexible or rigidinput:
output:Internal storage, robotics integration, sterility test pumps, or just-in-timeinput:
output:Positive pressure mode, which can be reversed if necessary.H2O2 or PAA integrated biodecontamination systeminput:
output:Turbulent, laminar, or unidirectional airflowinput:
output:Secure transfer system of the RTP type for residue managementinput:
output:Flexible containers for waste managementinput:
output:Compatible with a variety of drug management solutions, including digital or gravimetric control
output:Sterisafe® isolators guarantee personnel protection and containment. The "moving forward" principle is upheld, and each production operation (including the output of finished products, the removal of waste and remainders, and the management of remainders) adheres to a designated circuit to mitigate the risk of cross-contamination.input:
output:The HEPA filtered air flow (turbulent, unidirectional, or laminar) and the pressure mode are customized to your specific application in accordance with the recommendations and standards for isolation technology in healthcare institutions.input:
output:Sterisafe® isolators have been developed in close collaboration with our end users. Work ergonomics are optimized with a variety of standard comfort features.
input:
output:Our designers are delighted to assist you in the customization and configuration of your equipment to meet your requirements.input:
output:Modular design: Two gloves or two pairs of gloves in a line or face-to-faceinput:
output:Structure that is either flexible or rigidinput:
output:Internal storage, robotics integration, sterility test pumps, or just-in-timeinput:
output:Positive pressure mode, which can be reversed if necessary.H2O2 or PAA integrated biodecontamination systeminput:
output:Turbulent, laminar, or unidirectional airflowinput:
output:Secure transfer system of the RTP type for residue managementinput:
output:Flexible containers for waste managementinput:
output:Compatible with a variety of drug management solutions, including digital or gravimetric control
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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