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Overview of the CliniMACS Plus System and its therapeutic applications.
Details for recording instrument serial and model numbers for support.
Explains the meaning of icons used for warnings and notices in the manual.
Lists and explains various safety and product labeling symbols used in the document.
Defines key terms and components related to the CliniMACS Plus System and its operation.
Provides critical safety guidelines for operating the CliniMACS Plus Instrument.
States the instrument's status as a medical device in Europe and advises on checking status elsewhere.
Defines the system's purpose for in vitro separation of specific human cells for clinical applications.
Lists key specifications including model, dimensions, weight, power, and operating conditions.
Details the power connection module and main switch for different instrument models.
Provides instructions and warnings related to unpacking the instrument safely and inspecting for damage.
Offers guidance and warnings for safe transport, including chemical/biological hazards and ergonomic considerations.
Advises on safe placement of the instrument to prevent electrical hazards, overheating, and falling.
Instructs on proper cleaning procedures to avoid damage, electrical hazards, and maintain performance.
Explains that the instrument has no user-serviceable parts and requires professional maintenance.
Guides on the proper disposal of the instrument according to WEEE directives.
Details the key components and functions of the CliniMACS Plus Instrument.
Provides instructions for installing the CliniMACS Plus Instrument.
Explains the language selection and service menu options available for instrument configuration.
Describes the CliniMACS Plus Instrument as an electromechanical device.
Details the composition and nature of CliniMACS Reagents.
Explains the purpose and design of sterile, single-use tubing sets.
Describes the function of the PBS/EDTA buffer as a wash and transport fluid.
Notes that additional materials might be needed for separation, referencing the Application User Manual.
Provides contact information for technical support in case of instrument malfunctions or process failures.
Explains how error messages are displayed and what actions to take, usually contacting support.
Outlines the terms and conditions of the product warranty and limitations.
Lists registered trademarks and other trademarks associated with Miltenyi Biotec products.
Details EMC compliance and precautions for medical electrical equipment.
Provides guidance on electromagnetic immunity levels and environment for the instrument.
General| Brand | Miltenyi Biotec |
|---|---|
| Model | CliniMACS Plus |
| Category | Laboratory Equipment |
| Language | English |
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