Operating Room Control Panel
| Applications | For Operating Rooms |
| Other Characteristics | With Touchscreen |
| Applications | Containment, For Api, For Hpapi, For Cytotoxics, Dispensing, Transfer, For Quality Control, Sampling, For Powder Handling, Weigh, For Research And Development, Synthesis, Drying |
| Other Characteristics | Glove Box, With Hepa Filter, Stainless Steel, Negative Pressure, Custom, Controlled Atmosphere, Vacuum, Interface, Total Exhaust |
| Class | Class Ii |
| Configuration | Floor-Standing, Modular |
Associated tags
Product review
Catalog record
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Product summary
The Analytical Testing Isolator System has been specifically engineered for pharmaceutical industries that necessitate the highest levels of containment during the manipulation of potentially hazardous compounds (HAPIs).
The Isolator System is a GMP Class 2 containment enclosure that consists of an inlet/outlet airlock and a working chamber that accommodates four gloves.
The isolator incorporates a continuous liner and an RTP. Additionally, the isolator is equipped with a Wash-In-Place (WIP) system for manual washing operations.input:
output:
OPTIMUM SAFETY
The primary characteristic of a containment isolator is to optimize operator protection. A perfect combination of design and manufacturing strategies ensures that the Tema Sinergie Analytical Testing Isolator System maintains extremely stringent containment levels (≤50ng /m3). To ensure air tightness Class II (ISO 10648:2), the system is equipped with static and/or inflatable seals composed of FDA-approved EPDM (Ethylene Propylene Diene Monomer). The Analytical Testing Isolator System is the ideal adaptable solution for a variety of applications, including the weighing and dispensing of High Potent Active Pharmaceutical Ingredients (HPAPI), manual sampling, and product transfer.input:
output:
MODULAR BASED CONFIGURATIONinput:
output:
The system is designed with a modular approach that is both adaptable and flexible. The initial configuration of the isolator consists of a single working chamber that can be easily added to with additional chambers and/or airlocks. This renders the Analytical Testing Isolator System optimally suited to any process or requirement. A limited number of options may be implemented at a later date.
The Isolator System is a GMP Class 2 containment enclosure that consists of an inlet/outlet airlock and a working chamber that accommodates four gloves.
The isolator incorporates a continuous liner and an RTP. Additionally, the isolator is equipped with a Wash-In-Place (WIP) system for manual washing operations.input:
output:
OPTIMUM SAFETY
The primary characteristic of a containment isolator is to optimize operator protection. A perfect combination of design and manufacturing strategies ensures that the Tema Sinergie Analytical Testing Isolator System maintains extremely stringent containment levels (≤50ng /m3). To ensure air tightness Class II (ISO 10648:2), the system is equipped with static and/or inflatable seals composed of FDA-approved EPDM (Ethylene Propylene Diene Monomer). The Analytical Testing Isolator System is the ideal adaptable solution for a variety of applications, including the weighing and dispensing of High Potent Active Pharmaceutical Ingredients (HPAPI), manual sampling, and product transfer.input:
output:
MODULAR BASED CONFIGURATIONinput:
output:
The system is designed with a modular approach that is both adaptable and flexible. The initial configuration of the isolator consists of a single working chamber that can be easily added to with additional chambers and/or airlocks. This renders the Analytical Testing Isolator System optimally suited to any process or requirement. A limited number of options may be implemented at a later date.
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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