Class I product definition

Class I product means a complete aircraft, aircraft engine or propeller, which –
Class I product means: A DNA construct which is, or is intended to be, used to alter a mammalian cell so that said mammalian cell (i) carries a genetic modification resulting from the insertion of the said DNA construct targeted to a predetermined, specific chromosomal location without the intent to alter the function or expression of the gene(s) at the site of the targeted chromosomal location; and
Class I product means a complete aircraft, aircraft engine, RPS, or a propeller, which has been type certificated or is identical to a product type certificated in accordance with the provisions of these regulations;”; (h) the insertion after the definition of “cloud ceiling” of the following definition:

Examples of Class I product in a sentence

  • The luminaries offered shall conform to Level-1 classification, solidly grounded Class I product for Earthing.

  • A Class II product is a major component of a Class I product (e.g., wings, fuselages, empennage assemblies, landing gears, power transmissions, control surfaces, etc), the failure of which would jeopardize the safety of a Class I product; or any part, material, or appliance, approved and manufactured under the Technical Standard Order (TSO) system in the “C” series.

  • An appropriately Approved Maintenance Organization (AMO) having adequate overhaul facilities, and maintenance organization appropriate to the product involved, when the product is a Class I product located in a foreign country and has the approval by the Authority.

  • While this is a Class I product, provided with a protective earthing conductor in a power cord, an external protective earthing terminal has also been provided.

  • A Class II product is a major com- ponent of a Class I product (e.g., wings, fuselages, empennage assemblies, land- ing gears, power transmissions, control surfaces, etc), the failure of which would jeopardize the safety of a Class I product; or any part, material, or ap- pliance, approved and manufactured 14 CFR Ch. I (1–1–10 Edition)under the Technical Standard Order (TSO) system in the ‘‘C’’ series.

  • The fee also does not apply to any sale of a Class I product or any sale of a Class II product that is primarily sold to consumers at retail for not more than $100 per unit (under the FDA product classification system).

  • Parts are eligible for installation on : Make and model of Class I product : ________________________ Spec.

  • A person must apply for an export certificate of airworthiness for a Class I product that is a complete aircraft in the way set out in this regulation.

  • An appropriately certificated for- eign repair station having adequate overhaul facilities, and maintenance organization appropriate to the prod- uct involved, when the product is a Class I product located in a foreign country and an international office of Flight Standards Service has approved the use of such foreign repair station.

  • Issue of type acceptance certificate 21.04.5 (1) The Executive Director must grant an application in terms of regulation 21.04 2 and issue a type acceptance certificate for a Class I product if the applicant complies with the provisions of regulations 21.04.3 and 21.04.4. (2) A type acceptance certificate may be issued in both the standard and restricted categories referred to in regulation 21.04.1, if the provisions of regulations 21.04 3 and21.04.4 for each category are complied with.


More Definitions of Class I product

Class I product means: A DNA construct which is, or is intended to be, used to alter a mammalian cell so that said mammalian cell (i) carries a genetic modification resulting from the insertion of the said DNA construct targeted to a predetermined, specific chromosomal location without the intent to alter the function or expression of the gene(s) at the site of the targeted chromosomal location; and (ii) is or is intended to be used to create a line of mammalian animals. For clarity, Class I Product includes the said DNA construct (the “Class I Construct”), the said altered mammalian cell and the said altered mammalian animal line. Class I Product only includes the insertion of DNA sequences that are not intended to (a) alter the function or expression of the gene(s) at the site of the targeted chromosomal location, or (b) have a phenotypic impact on the said altered mammalian animal line. Examples of DNA sequences which can be inserted in ways that would not alter the function or expression of the gene(s) at the site of the targeted chromosomal location and thus would be expected not to have a phenotypic impact, are those encoding reporter proteins such as GFP or lacZ cell surface markers, protein tags or trans- acting utility proteins, such as recombinases including Cre and FLP recombinases, but do not include libraries of cDNAS to be screened for phenotypic effects of their misexpression. For clarity, a Class I product is commonly known as “conditional knock-outs”, “reporter strains”, “cell-surface markers”, “protein tagging”, “transacting utility proteins” (such as Cre, Flp, or Fre Recombinase).
Class I product means a complete aircraft, aircraft engine, RPS, or a propeller, which has been type certificated or is identical to a product type certificated in accordance with the provisions of these regulations;”;

Related to Class I product

  • Anti-Static Product means a product that is labeled to eliminate, prevent, or inhibit the accumulation of static electricity. “Anti-Static Product” does not include “Electronic Cleaner,” “Floor Polish or Wax,” “Floor Coating,” and products that meet the definition of “Aerosol Coating Product” or “Architectural Coating.”

  • Licensed Product means a product, method or service in the Licensed Field of Use, the making, having made, using, importing or selling of which, absent this license, infringes, induces infringement, or contributes to infringement of a Licensed Patent.

  • Hemp product means the same as that term is defined in § 3.2-4112.

  • Drug Product means a specific drug in dosage form from a known source of manufacture, whether

  • Diagnostic Product means any test or assay for diagnosing or detecting a disease, disorder, medical condition, or symptom.

  • Tobacco product means any substance containing tobacco leaf, including but not limited to, cigarettes, cigars, pipe tobacco, hookah tobacco, snuff, chewing tobacco, dipping tobacco, bidis, blunts, clove cigarettes, or any other preparation of tobacco; and any product or formulation of matter containing biologically active amounts of nicotine that is manufactured, sold, offered for sale, or otherwise distributed with the expectation that the product or matter will be introduced into the human body by inhalation; but does not include any cessation product specifically approved by the U.S. Food and Drug Administration for use in treating nicotine or tobacco dependence.

  • Collaboration Product means a pharmaceutical product containing or comprising Compound in any dosage form alone, or in combination with, one or more other pharmaceutically active ingredients, and any and all Improvements thereto.

  • Combination Product means any product that comprises a Licensed Compound or Licensed Product sold in conjunction with another active component so as to be a combination product (whether packaged together or in the same therapeutic formulation).

  • Milk product or "dairy product" means cottage cheese, dry curd cottage cheese, reduced fat cottage cheese, lowfat cottage cheese, cream, light cream, light whipping cream, heavy cream, heavy whipping cream, whipped cream, whipped light cream, sour cream, acidified sour cream, cultured sour cream, half-and-half, sour half-and-half, acidified sour half-and-half, cultured sour half-and-half, reconstituted or recombined milk and milk products, concentrated milk, concentrated milk products, skim milk, lowfat milk, frozen milk concentrate, flavored milk, eggnog, buttermilk, cultured milk, cultured lowfat milk, cultured skim milk, yogurt, lowfat yogurt, nonfat yogurt, acidified milk, acidified lowfat milk, acidified skim milk, low-sodium milk, low-sodium lowfat milk, low-sodium skim milk, lactose-reduced milk, lactose-reduced lowfat milk, lactose-reduced skim milk, aseptically processed and packaged milk, milk products with added safe and suitable microbial organisms, and any other milk product made by the addition or subtraction of milkfat or addition of safe and suitable optional ingredients for protein, vitamin, or mineral fortification. Unless a product is considered a milk product under this subdivision, milk product does not include dietary products, infant formula, ice cream or other desserts, cheese, or butter. Milk products include the following:

  • Bundled Product means Product sold together with any other product(s) or service(s) at a single unit price, whether packaged together or separately, and which other product(s) or service(s) have material independent value from Product itself.

  • Marihuana-infused product means a topical formulation, tincture, beverage, edible substance, or similar product containing marihuana and other ingredients and that is intended for human consumption.

  • Recycled product means a product containing recovered material, or post-consumer recovered material, or both.

  • Licensed Compound means [***].

  • Generic Product means any pharmaceutical product that (i) is sold by a Third Party that is not an Affiliate or licensee of Buyer and (ii) (a) contains the same active pharmaceutical ingredient as the Product or (b) is categorized by the applicable Governmental Entity in a country to be therapeutically equivalent to, or interchangeable with, the Product, such that the pharmaceutical product may be substituted for the Product at the point of dispensing without any intervention by the prescribing physician in such country.

  • Reference biological product means the single biological product licensed pursuant to 42 U.S.C.

  • Biological product means a virus, therapeutic serum, toxin, antitoxin, vaccine, blood, blood component or derivative, allergenic product, protein other than a chemically synthesized polypeptide, or analogous product, or arsphenamine or any derivative of arsphenamine or any other trivalent organic arsenic compound, applicable to the prevention, treatment, or cure of a disease or condition of human beings.

  • New Product means the Synology-branded hardware product and Synology-branded accessories contained in the original packaging Customer bought from an authorized Synology distributor or reseller. You may see our “New Product” at Product Support Status.

  • Interchangeable biological product means a biological product that the U.S. Food and Drug Administration has:

  • Edible cannabis product means cannabis product that is intended to be used, in whole or in part, for human consumption, including, but not limited to, chewing gum, but excluding products set forth in Division 15 (commencing with Section 32501) of the Food and Agricultural Code. An edible cannabis product is not considered food, as defined by Section 109935 of the Health and Safety Code, or a drug, as defined by Section 109925 of the Health and Safety Code.

  • Roll-on product means any antiperspirant or deodorant that dispenses active ingredients by rolling a wetted ball or wetted cylinder on the affected area.

  • Clinical Trial means a Phase I Clinical Trial, Phase II Clinical Trial or Phase III Clinical Trial, or any post-approval human clinical trial, as applicable.

  • Derivative Product means a written contract or agreement between the Authority and a Reciprocal Payor, which provides that the Authority’s obligations thereunder will be conditioned on the absence of (a) a failure by the Reciprocal Payor to make any payment required thereunder when due and payable, or (b) a default thereunder with respect to the financial status of the Reciprocal Payor; and:

  • Competing Product means […***…].

  • complex product means a product which is composed of multiple components which can be replaced permitting disassembly and re-assembly of the product.

  • Compound means the taking of two or more ingredients and fabricating them into a single

  • Back-Up Compound means, with reference to any particular Development Candidate or Drug Product Candidate, a Compound which (a) has the same principal mode of action (i.e., Potentiator or Corrector) as that Development Candidate or Drug Product Candidate; and (b) was among the group of Compounds, identified by VERTEX as potential additional lead molecules having the same principal mode of action, from which the Development Candidate was selected.