TSI CERTIFIER FA PLUS 4088 INTERFACE MODULE FLOW ANALYSER.
The TSI 4088 Certifier Fa Plus, Interface Module is a cutting-edge technology developed by TSI. This module is designed to enhance the functionality of the TSI 4088 Certifier Fa Plus, a highly reliable airflow capture hood used in HVAC testing and balancing applications. The interface module serves as a bridge between the Certifier Fa Plus and various other devices, allowing for seamless integration and data exchange.
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Model: TSI 4088 Certifier Fa Plus
Interface Module: TSI / Alnor
Compatible with TSI 4088 Certifier Fa Plus model
Designed to connect TSI 4088 Certifier Fa Plus to Alnor instruments
Allows data transfer and communication between the Certifier Fa Plus and Alnor devices
Enables seamless integration of TSI and Alnor equipment for comprehensive testing and analysis
Provides accurate and reliable measurement data for various parameters such as airflow, pressure, temperature, and velocity
Easy to install and use, with user-friendly interface and intuitive controls
Robust and durable construction, ensuring long-term performance and reliability
Complies with TSI and Alnor specifications and quality standards
DISCLAIMER: All medical items are sold in good clean functioning condition unless otherwise stated. It is the buyers responsibility to have the item professionally tested, calibrated or serviced before clinical use on humans or animals.
NOTE: Regardless of the origin of the equipment, documentation provided or identification appearing upon the equipment, the equipment described and offered here is in no way certified for, recommended for, or offered for any specific use. The purchaser agrees that the seller shall not be held responsible or liable for any injuries or damages, whether incidental or consequential, associated in any way with the equipment. The purchaser, by offering on this equipment, indicates their acknowledgment of, and agreement to the terms of this disclaimer.
CE MARKED - This product is in compliance with the essential requirements of Council Directive 93/42/EEC Medical Device Directive, as amended by Council Directive 2007/47/EC, class IIa
NOTE: The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. If so, do not bid on this item unless you are an authorized purchaser. If the item is subject to FDA regulation, We will verify your status as an authorized purchaser of this item before shipping of the item.
