Product Definition. The term PRODUCTS, as used herein, shall refer only to PRODUCTS as identified in Exhibit A.
Product Definition. “Product” shall mean products in the Supplier’s product assortment and/or services requested by the Buyer and which are specified in the PO (the “Products”). In addition, any reference to “Service” in these GTC shall refer to the aforementioned services, forming part of the Products unless otherwise explicitly agreed. The terms in these GTC shall apply to the Services, as applicable.
Product Definition. The term "Product" shall be defined to mean only aseptic packaged product (not extended shelf life container product or fresh serve container product), produced by Nordic for Hain or for the Westsoy products of Hain, or for the private label business of Hain, or for any Heinz business, or for any affiliate of Hain, and produced in the size and flavors specified in Exhibit A attached hereto, which Exhibit may be updated and revised from time to time by the parties. For purposes of this Agreement, "affiliate" shall mean any individual, partnership, limited liability company, limited liability partnership, corporation, trust or other entity which is owned or controlled by a party hereto, or which owns or controls a party hereto, or is under the common control of a party hereto.
Product Definition. At the start of this Agreement, Supplier shall produce the Products defined in Appendix "A" exactly to the drawings, specifications, and documentation provided by Netrx xxx agreed to in writing by Supplier unless otherwise approved in writing by Netrx. Xxly the suppliers shown on the Approved Vendor List ("AVL") provided by Netrx xxxll be utilized for the initial procurement of materials. Supplier shall have the right to submit revisions to Netrx xx the AVL and Bill xx Material ("BOM") so that cost reductions shall be achieved. Such revisions may include, but not be limited to design changes, manufacturing technology improvements, development of new vendors, etc. All such changes submitted by Supplier shall be approved in writing by Netrx, xxior to implementation of the changes and Netrx xxxll have the unlimited right to use such changes, in any way it deems appropriate and at its sole discretion.
Product Definition. The Product is defined in Exhibit A, and includes CBD Extraction Equipment in commercial and private cannabis industries.
Product Definition. [***] Caprolactam, [***] and [***] Polymer shall be referred to herein collectively as “Product”. The parties agree that, at Seller’s sole discretion, Seller may [***].
Product Definition. The XXXX Medical Systems, Inc. Model 1500 Series Electrosurgical Generator is designed to provide monopolar radiofrequency energy to be used for coagulation and ablation of soft tissue. The unit is specifically designed for use with XXXX Electrosurgical Devices. It provides multiple temperature sensor measurements, impedance and power monitoring to assist the practitioner in delivering the desired energy to the target tissue. The XXXX Electrosurgical system consists of an RF generator, a disposable electrode, here referred to as the device, a patient connection cable, a return pad, a power cord, and may also include an auxiliary temperature probe. The generator provides the RF energy to the device through the cable. The device consists of a number of deployable branches, some or all equipped with a thermocouple. The return pad also known as the dispersive electrode, provides the return path for the RF energy applied by the device. The power cord is a medical grade line cord that provides AC power to the generator. The system is capable of reading up to three auxiliary temperatures through a passive auxiliary probe. This probe is not capable of delivering any RF energy, and is used to provide temperature information about the surrounding tissue. This probe is connected to the auxiliary port of the generator via an auxiliary cable. To use the system, the generator is plugged into the wall outlet. The device is connected to the generator via the patient connection cable. The dispersive electrode is placed on the appropriate location on the body and connected to its port on the generator. Once the system is successfully powered up, the user can set the parameters of the procedure such as the mode of operation, procedure time, procedure temperature, and the power delivery level. With the device placed in the tissue to be ablated and its electrodes deployed, RF can be turned on. The system parameters are continuously monitored and reported by the generator. If the measured parameters are outside the acceptable limits the RF energy delivery stops and a message appears on the LCD display. The RF energy delivery ceases once the procedure is completed based on the initial user defined parameters.
Product Definition. The PRODUCT is the Trichlorosilane material leaving the LICENSED UNIT having the average properties listed below: Acceptors [*] [*] [*] Donors [*] [*] [*] [*] [*] [*] [*] [*] [*] [*] [*] [*] [*] [*] [*] [*] [*] [*] [*]
Product Definition. 1.1 SAC shall use its best efforts to provide technical support to the following products (the "Products") for the benefit of Inter-Con:
Product Definition. As used in this Agreement, the term "PRS" shall mean the products developed and manufactured by the Company which are identified in Schedule B attached to and made a part of this Agreement and also such products ---------- hereafter developed and made by the Company as improved or successor models of or to such products.
