Section 22-B10204. LICENSING PROCEDURES FOR DISTRIBUTORS, MANUFACTURERS, INITIAL IMPORTERS AND VENDORS  


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    10204.1License application forms may be obtained from the Department at 899 North Capitol Street, N.E., Washington, D.C., or online at www.hpla.doh.dc.gov.

     

    10204.2The application for licensure as a medical device distributor, manufacturer, initial importer, or vendor shall be signed and verified, and submitted on a license application form furnished by the Department.

     

    10204.3If the legal entity is a proprietorship, partnership, corporation, or association, the application shall contain the following:

     

    (a)The name and residence address of the applicant, and the date and place of  incorporation (if applicable);

     

    (b)The name and address of the corporation’s registered agent and  corporation charter number, or if any other type of association;

     

    (c)The names of the principals of such association; 

     

    (d)The name of the legal entity to be licensed, including the name under  which the business is conducted;

     

    (e)The address of each place of business that is licensed;

     

    (f)If a proprietorship, the name and residence address of the proprietorship;

     

    (g)If a corporation, the date and place of incorporation and name and address  of its registered agent in the state and corporation charter number; or

     

    (h)If any other type of association, the names of the principals of such  association;

     

    (i)The name, residence address, and valid driver’s license number of each  individual in an actual administrative capacity which, in the case of  proprietorship, shall be the managing proprietor; partnership, the  managing partner; corporation, the officers and directors; or those in a  managerial capacity in any other type of association; and

     

    (j)For each place of business, the residence address of the individual in  charge;

     

    10204.4A completed application shall entitle a medical device distributor, manufacturer, initial importer, or vendor to a license, except as provided in § 10207.

    10204.5The renewal application for licensure as a medical device distributor, manufacturer, initial importer, or vendor shall be made on a license application form furnished by the Department. 

     

     

authority

Sections 4902(a) (8) and 4908 of the Department of Health Functions Clarification Act of 2001, effective October 3, 2001 (D.C. Law 14-28; D.C. Official Code §§ 7-731(a)(8) and 7-737 (2012 Repl. & 2016 Supp.)), and Mayor’s Order 2006-34, dated March 12, 2006.

source

Final Rulemaking published at 60 DCR 10252 (July 12, 2013); as amended by Final Rulemaking published at 63 DCR 13491 (October 28, 2016).