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 D.C. Municipal Regulations (Last Updated: September 13, 2017)
 Title 22. HEALTH
 SubTilte 22-B. PUBLIC HEALTH AND MEDICINE
 Chapter 22-B108. PERFORMANCE STANDARDS FOR ELECTRONIC PRODUCTS (GENERAL), IONIZING RADIATION EMITTING PRODUCTS, LIGHT-EMITTING PRODUCTS, AND SONIC, INFRASONIC, AND ULTRASONIC RADIATION EMITTING PRODUCTS

  Section 22-B10813. DISPOSITION OF RECORDS OBTAINED BY DEALERS AND DISTRIBUTORS  

Latest version.

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    10813.1Information obtained by dealers and distributors pursuant to § 10812 shall immediately be forwarded to the appropriate manufacturer unless:

     

    (a) The dealer or distributor elects to hold and preserve such information and to immediately furnish it to the manufacturer when advised by the manufacturer or the Department of Health, that such information is required; and

     

    (b) The dealer or distributor, upon making the election under § 10813.1(a) of this section, promptly notifies the manufacturer of such election.  Such notification shall be in writing and shall identify the dealer or distributor and the electronic product or products for which the information is being accumulated and preserved.

     

    10813.2Every dealer or distributor who elects to hold and preserve information required pursuant to § 10812 shall preserve the information for a period of five (5) years from the date of the sale, award, or lease of the product, or until the dealer or distributor discontinues dealing in, or distributing the product, whichever is sooner. If the dealer or distributor discontinues dealing in, or distributing the product, such information as obtained pursuant to § 10812 shall be furnished at that time, or before, to the manufacturer of the product.

     

authority

Section 19(a)(3) of the District of Columbia Pharmacist and Pharmacy Regulation Act of 1980, effective September 16, 1980 (D.C. Law 3-98; D.C. Official Code § 47-2885.18(a)(3) (2005 Repl.)); Mayor’s Order 98-48, dated April 15, 1998; Section 4902 of the Fiscal Year 2002 Budget Support Act of 2001, effective October 3, 2001 (D.C. Law 14-28; D.C. Official Code § 7-731 (2008 Repl.)); Section 15 of the District of Columbia Medical Device Manufacture and Distribution Licensure Act of 1990, effective June 13, 1990 (D.C. Law 8-137; D.C. Official Code § 48-714(a) (2005 Repl.)); and Mayor’s Order 98-88, dated May 29, 1998.

source

Final Rulemaking published at 60 DCR 10252 (July 12, 2013).