Product Manual definition

Product Manual means the Listing and Approved Prices for Limb Prostheses.
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Product Manual means the Listing and Approved Prices for Orthotic Devices.
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Product Manual means the Product Manual – Visual Aids
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Examples of Product Manual in a sentence

  • Free Set of Activities – The set of Products workflow actions and conditions listed at the Appendix A of the Product Manual.

  • Leukapheresed cells obtained at participating centers will be shipped to the cell processing facility (CPF) overnight as described in the Investigational Product Manual.

  • Each subject who enters the screening period will receive a unique subject identification number at the time of consent [refer to the Investigational Product Manual (IPM)].

  • LIMITED WARRANTY: - SCAN SYS warrants that (a) the SOFTWARE will perform substantially in accordance with the accompanying Product Manual for a period of 90 days from the date of receipt; and (b) any SCAN SYS supplied hardware accompanying the SOFTWARE will be free from defects in materials and workmanship under normal use and service for a period of one year from the date of receipt.

  • ProSign warrants that the iCon-L ®-Software will perform substantially in accordance with the accompanying Product Manual for a period of 6 months from the date of purchase.

  • Defect” refers to when the Product does not correspond with the specifications given in the Product Manual, which results in that the Product cannot be used or in an considerable limitation of the use of the Product.

  • This Warranty does not apply to Products damaged by wind, gusts or squalls in excess of the wind class rating as specified in the Product Manual.

  • REQ-028809/A REQ-028814/A REQ-028810/A The Supplier shall provide the Product Manual as part of the delivered Device.

  • In order to be covered by the Service Plan, the unit must be under Promise Warranty and not have been subjected to abuse or conditions outside the environmental specifications recommended in Promise Product Manual (User Guide).

  • The Folding Arm Awning and External Roller Blinds systems have a wind class rating specified in the Product Manual of each system.


More Definitions of Product Manual

Product Manual means the Listed Devices and Approved Prices for Maxillofacial Intraoral Prostheses.
Sample 1
Product Manual means the Listed Devices and Approved Prices for Ocular Prostheses.
Sample 1
Product Manual means the instructions and manuals issued by Pylontech with the Product that set out how the Product should be installed and operated.
Sample 1
Product Manual means Collexia supplied user manual either in hard copy or published in the Collexia Payments Product; which describes the functions supported in the product including the applicable business and Clearing Rules per product selected and where the Product Manual supplied or published forms an integral part of this Agreement and where the Product Manual amplifies all such arrangements between the parties in accordance with the terms hereof. The Product Manual is copyright protected and forms part of the confidential information as described herein;
Sample 1
Product Manual means the compilation of formulations. Specifications and procedures (including but not limited to recall procedures), quality controls, packaging and handling for the Product, developed by MERISANT as set forth in the attached Exhibit l.l(c), which may be amended from time to time by MERISANT.
Sample 1

Related to Product Manual

  • Program Manual means the United States Department of Agriculture, Animal and Plant Health Inspection Service, Plant Protection and Quarantine, Gypsy Moth Program Manual, 1994 edition.

  • Project Manual means the volume usually assembled for the Work which may include the bidding requirements, sample forms, and other Contract Documents.

  • Product Manufacturer means the entity that assembles the component parts to manufacture the final Product;

  • Procurement Manual means the Procurement Manual set forth as chapter 4 of the PIP (as hereinafter defined), which Manual sets forth the procurement management and institutional arrangements and obligations under the Project as such Manual may be amended from time to time by agreement between the Association and Recipient.

  • Diagnostic clinical procedures manual means a collection of written procedures that describes each method (and other instructions and precautions) by which the licensee performs diagnostic clinical procedures; where each diagnostic clinical procedure has been approved by the authorized user and includes the radiopharmaceutical, dosage, and route of administration.

  • Design Manual means the MOHLTC design manual or manuals in effect and applicable to the development, upgrade, retrofit, renovation or redevelopment of the Home or Beds subject to this Agreement.

  • labelling means any words, particulars, trade marks, brand name, pictorial matter or symbol relating to a food and placed on any packaging, document, notice, label, ring or collar accompanying or referring to such food;

  • Tobacco product manufacturer means an entity that after the date of enactment of this Act directly (and not exclusively through any affiliate):

  • Contract Manufacturer means a company that produces goods under contract for another company under the label or brand name of that company.

  • User Manual means the user guide, Help Guide, documentation provided with the Software, updated agreements provided on the website of Quick Heal (xxx.xxxxxxxxx.xxx), explanatory or other materials as provided from time to time by Quick Heal.

  • Product Specifications means the specifications, features and/or terms of any "Contract" (as defined in the LME Rules) listed for trading on the LME, as described in the LME Rules;

  • Product Schedule means PTC’s standard order form entitled “PTC Product Schedule” (including all schedules, attachments and other document(s) specifically referenced therein) or such alternative order form as may be submitted by Customer and accepted by PTC, in each case that specifies (i) the Licensed Products and/or Services ordered; and (ii) for Licensed Products, the installation address (including the Designated Country) and the Licence Term.

  • Program Materials means the documents and information provided by the Program Administrator specifying the qualifying EEMs, technology requirements, costs and other Program requirements, which include, without limitation, program guidelines and requirements, application forms and approval letters.

  • Product Specification means a product specification for a Medical Device set out in Schedule 2;

  • Manufacturing Process means any process for—

  • Brand Name Specification means a specification limited to one or more items by manufacturers’ names or catalogue number.

  • Technical safeguards means the technology and the policy and procedures for its use that 27 protect electronic PHI and control access to it.

  • Procedures Manual means the standards and procedures manual described in Section 11.3.

  • Product Labeling means, with respect to a Licensed Product in a country or other jurisdiction in the Territory, (a) the Regulatory Authority-approved full prescribing information for such Licensed Product for such country or other jurisdiction, including any required patient information, and (b) all labels and other written, printed, or graphic matter upon a container, wrapper, or any package insert utilized with or for such Licensed Product in such country or other jurisdiction.

  • Product Terms means the document that provides information about Microsoft Products and Professional Services available through volume licensing. The Product Terms document is published on the Licensing Site and is updated from time to time.

  • Protocols means written directions and orders, consistent with the department’s standard of care, that are to be followed by an emergency medical care provider in emergency and nonemergency situations. Protocols must be approved by the service program’s medical director and address the care of both adult and pediatric patients.

  • Provider Manual means a working document, including but not limited to BCBSM published bulletins and provider notices, that provide specific guidelines and direction by which providers may meet their contractual responsibility as described in this Agreement. Provider Manuals are published on web-DENIS.

  • Active Pharmaceutical Ingredient or “API” shall mean one or more of the following active pharmaceutical ingredients: tenofovir alafenamide (“TAF”), tenofovir disoproxil fumarate (“TDF”), elvitegravir (“EVG”), and cobicistat (“COBI”).

  • Manufacturing Materials means parts, tools, dies, jigs, fixtures, plans, drawings, and information produced or acquired, or rights acquired, specifically to fulfill obligations set forth herein.

  • Protocol means, in respect of any category of object and associated rights to which this Convention applies, the Protocol in respect of that category of object and associated rights;

  • technical specification means, with respect to any Software, the document setting forth the technical specifications for such Software and included in the Statement of Work.