{"formats":[{"name":"JSON","format":"json","url":"\/downloads\/2025\/code-json\/54.1-3435.3_1.json"},{"name":"Plain Text","format":"text","url":"\/downloads\/2025\/code-text\/54.1-3435.3_1.txt"},{"name":"XML","format":"xml","url":"\/downloads\/2025\/code-xml\/54.1-3435.3_1.xml"},{"name":"HTML","format":"html","url":"\/downloads\/2025\/code-html\/54.1-3435.3_1.html"}],"law_id":58671,"edition_id":1,"section_id":58671,"structure_id":13241,"section_number":"54.1-3435.3:1","catch_line":"Registration of nonresident medical equipment suppliers; renewal; fee","history":"2016, c. 88.","full_text":"A\n\nAny person located outside the Commonwealth other than a nonresident pharmacy registered pursuant to § 54.1-3434.1 that ships, mails, or delivers to a consumer in the Commonwealth any hypodermic syringes or needles, medicinal oxygen, Schedule VI controlled device, those Schedule VI controlled substances with no medicinal properties that are used for the operation and cleaning of medical equipment, sterile water and saline for irrigation, or solutions for peritoneal dialysis pursuant to a lawful order of a prescriber shall be registered with the Board as a nonresident medical equipment supplier. Registration as a nonresident medical equipment supplier shall be renewed by March 1 of each year. Applicants for registration or renewal of a registration shall submit a fee specified by the Board in regulations at the time of registration or renewal. A nonresident medical equipment supplier registered in accordance with this section shall notify the Board within 30 days of any substantive change in the information previously submitted to the Board.B\n\nThe nonresident medical equipment supplier shall at all times maintain a valid, unexpired license, permit, or registration in the state in which it is located, if required by the resident state, and shall furnish proof of such license, permit, or registration upon application for registration or renewal. If the resident state does not require a license, permit, or registration to engage in direct consumer supply of the medical equipment described in subsection A, the applicant shall furnish proof that it meets the minimum statutory and regulatory requirements for medical equipment suppliers in the Commonwealth.C\n\nRecords of distribution of medical equipment described in subsection A into the Commonwealth shall be maintained in such a manner that they are readily retrievable from records of distribution into other jurisdictions and shall be provided to the Board, its authorized agent, or any agent designated by the Superintendent of State Police upon request within seven days of receipt of such request.","order_by":null,"text":{"0":{"id":215020,"text":"Any person located outside the Commonwealth other than a nonresident pharmacy registered pursuant to § 54.1-3434.1 that ships, mails, or delivers to a consumer in the Commonwealth any hypodermic syringes or needles, medicinal oxygen, Schedule VI controlled device, those Schedule VI controlled substances with no medicinal properties that are used for the operation and cleaning of medical equipment, sterile water and saline for irrigation, or solutions for peritoneal dialysis pursuant to a lawful order of a prescriber shall be registered with the Board as a nonresident medical equipment supplier. Registration as a nonresident medical equipment supplier shall be renewed by March 1 of each year. Applicants for registration or renewal of a registration shall submit a fee specified by the Board in regulations at the time of registration or renewal. A nonresident medical equipment supplier registered in accordance with this section shall notify the Board within 30 days of any substantive change in the information previously submitted to the Board.","type":"section","prefixes":["A"],"prefix":"A","entire_prefix":"A","prefix_anchor":"A","level":1,"next_prefix":"B"},"1":{"id":215021,"text":"The nonresident medical equipment supplier shall at all times maintain a valid, unexpired license, permit, or registration in the state in which it is located, if required by the resident state, and shall furnish proof of such license, permit, or registration upon application for registration or renewal. If the resident state does not require a license, permit, or registration to engage in direct consumer supply of the medical equipment described in subsection A, the applicant shall furnish proof that it meets the minimum statutory and regulatory requirements for medical equipment suppliers in the Commonwealth.","type":"section","prefixes":["B"],"prefix":"B","entire_prefix":"B","prefix_anchor":"B","level":1,"prior_prefix":"A","next_prefix":"C"},"2":{"id":215022,"text":"Records of distribution of medical equipment described in subsection A into the Commonwealth shall be maintained in such a manner that they are readily retrievable from records of distribution into other jurisdictions and shall be provided to the Board, its authorized agent, or any agent designated by the Superintendent of State Police upon request within seven days of receipt of such request.","type":"section","prefixes":["C"],"prefix":"C","entire_prefix":"C","prefix_anchor":"C","level":1,"prior_prefix":"B"}},"ancestry":[{"id":13241,"edition_id":1,"name":"Wholesale Distributors and Medical Equipment Suppliers","identifier":"3","label":"article","depth":4,"order_by":1,"parent_id":13240,"metadata":{},"date_created":"2026-06-26 03:44:30","date_modified":"2026-06-26 03:44:30","permalink":{"id":243495,"object_type":"structure","relational_id":13241,"identifier":"3","token":"54.1\/III\/34\/3","url":"\/54.1\/III\/34\/3\/","edition_id":1,"permalink":0,"preferred":1}},{"id":13240,"edition_id":1,"name":"Drug Control Act","identifier":"34","label":"chapter","depth":3,"order_by":1,"parent_id":12758,"metadata":{},"date_created":"2026-06-26 03:44:30","date_modified":"2026-06-26 03:44:30","permalink":{"id":243223,"object_type":"structure","relational_id":13240,"identifier":"34","token":"54.1\/III\/34","url":"\/54.1\/III\/34\/","edition_id":1,"permalink":0,"preferred":1}},{"id":12758,"edition_id":1,"name":"Professions and Occupations Regulated by Boards Within the Department of Health Professions","identifier":"III","label":"subtitle","depth":2,"order_by":1,"parent_id":12754,"metadata":{},"date_created":"2026-06-26 03:43:51","date_modified":"2026-06-26 03:43:51","permalink":{"id":241105,"object_type":"structure","relational_id":12758,"identifier":"III","token":"54.1\/III","url":"\/54.1\/III\/","edition_id":1,"permalink":0,"preferred":1}},{"id":12754,"edition_id":1,"name":"Professions and Occupations","identifier":"54.1","label":"title","depth":1,"order_by":1,"parent_id":null,"metadata":{},"date_created":"2026-06-26 03:43:51","date_modified":"2026-06-26 03:43:51","permalink":{"id":239313,"object_type":"structure","relational_id":12754,"identifier":"54.1","token":"54.1","url":"\/54.1\/","edition_id":1,"permalink":0,"preferred":1}}],"structure_contents":[{"id":86023,"structure_id":13241,"section_number":"54.1-3435","catch_line":"License to act as wholesale distributor; renewal; fee","url":"\/54.1-3435\/","token":"54.1\/III\/34\/3\/54.1-3435","metadata":false},{"id":87353,"structure_id":13241,"section_number":"54.1-3435.01","catch_line":"Registration of nonresident wholesale distributors; renewal; fee","url":"\/54.1-3435.01\/","token":"54.1\/III\/34\/3\/54.1-3435.01","metadata":false},{"id":84340,"structure_id":13241,"section_number":"54.1-3435.02","catch_line":"Certain permitted pharmacies and medical equipment suppliers exempted","url":"\/54.1-3435.02\/","token":"54.1\/III\/34\/3\/54.1-3435.02","metadata":false},{"id":78139,"structure_id":13241,"section_number":"54.1-3435.1","catch_line":"Denial, revocation, and suspension of license, permit, or registration of certain entities","url":"\/54.1-3435.1\/","token":"54.1\/III\/34\/3\/54.1-3435.1","metadata":false},{"id":69203,"structure_id":13241,"section_number":"54.1-3435.2","catch_line":"Permit to act as medical equipment supplier; storage; limitation; regulations","url":"\/54.1-3435.2\/","token":"54.1\/III\/34\/3\/54.1-3435.2","metadata":false},{"id":69720,"structure_id":13241,"section_number":"54.1-3435.3","catch_line":"Inspection and audit","url":"\/54.1-3435.3\/","token":"54.1\/III\/34\/3\/54.1-3435.3","metadata":false},{"id":58671,"structure_id":13241,"section_number":"54.1-3435.3:1","catch_line":"Registration of nonresident medical equipment suppliers; renewal; fee","url":"\/54.1-3435.3_1\/","token":"54.1\/III\/34\/3\/54.1-3435.3_1","metadata":false},{"id":78752,"structure_id":13241,"section_number":"54.1-3435.4","catch_line":"Permit to act as warehouser; regulations","url":"\/54.1-3435.4\/","token":"54.1\/III\/34\/3\/54.1-3435.4","metadata":false},{"id":76533,"structure_id":13241,"section_number":"54.1-3435.4:01","catch_line":"Registration to act as a nonresident warehouser; regulations","url":"\/54.1-3435.4_01\/","token":"54.1\/III\/34\/3\/54.1-3435.4_01","metadata":false},{"id":66466,"structure_id":13241,"section_number":"54.1-3435.4:1","catch_line":"Permitting of third-party logistics provider; renewal","url":"\/54.1-3435.4_1\/","token":"54.1\/III\/34\/3\/54.1-3435.4_1","metadata":false},{"id":56810,"structure_id":13241,"section_number":"54.1-3435.4:2","catch_line":"Registration of nonresident third-party logistics provider; renewal","url":"\/54.1-3435.4_2\/","token":"54.1\/III\/34\/3\/54.1-3435.4_2","metadata":false},{"id":54243,"structure_id":13241,"section_number":"54.1-3435.5","catch_line":"Repealed","url":"\/54.1-3435.5\/","token":"54.1\/III\/34\/3\/54.1-3435.5","metadata":false},{"id":73025,"structure_id":13241,"section_number":"54.1-3436","catch_line":"Repealed","url":"\/54.1-3436\/","token":"54.1\/III\/34\/3\/54.1-3436","metadata":false},{"id":81429,"structure_id":13241,"section_number":"54.1-3436.1","catch_line":"Prescription drug price transparency","url":"\/54.1-3436.1\/","token":"54.1\/III\/34\/3\/54.1-3436.1","metadata":false}],"previous_section":{"id":69720,"structure_id":13241,"section_number":"54.1-3435.3","catch_line":"Inspection and audit","url":"\/54.1-3435.3\/","token":"54.1\/III\/34\/3\/54.1-3435.3","metadata":false},"next_section":{"id":78752,"structure_id":13241,"section_number":"54.1-3435.4","catch_line":"Permit to act as warehouser; regulations","url":"\/54.1-3435.4\/","token":"54.1\/III\/34\/3\/54.1-3435.4","metadata":false},"metadata":false,"official_url":"https:\/\/law.lis.virginia.gov\/vacode\/54.1-3435.3:1\/","history_text":"

This law was first created in 2016. The record of its establishment is cataloged in chapter 88<\/a> of that year\u2019s edition of \u201cActs of Assembly,\u201d the annual state publication listing all changes made to the Code of Virginia in that year.<\/p>","references":false,"refers_to":[{"id":77369,"section_number":"54.1-3434.1","catch_line":"Nonresident pharmacies to register with Board","order_by":null,"url":"\/54.1-3434.1\/"}],"permalink":{"id":243521,"object_type":"law","relational_id":58671,"identifier":"54.1-3435.3:1","token":"54.1\/III\/34\/3\/54.1-3435.3_1","url":"\/54.1-3435.3_1\/","edition_id":1,"permalink":0,"preferred":1},"url":"\/54.1-3435.3_1\/","token":"54.1\/III\/34\/3\/54.1-3435.3_1","dublin_core":{"Title":"Registration of nonresident medical equipment suppliers; renewal; fee","Type":"Text","Format":"text\/html","Identifier":"\u00a7 54.1-3435.3:1","Relation":"Code of Virginia"},"html":"\n\t\t\t\t\t\t

A.<\/span> Any person<\/span> located outside the Commonwealth other than a nonresident pharmacy registered pursuant to § 54.1-3434.1<\/a> that ships, mails, or delivers<\/span> to a consumer in the Commonwealth any hypodermic syringes or needles, medicinal oxygen, Schedule VI controlled device<\/span>, those Schedule VI controlled substances<\/span> with no medicinal properties that are used for the operation and cleaning of medical equipment, sterile water and saline for irrigation, or solutions for peritoneal dialysis pursuant to a lawful order<\/span> of a prescriber<\/span> shall be registered with the Board<\/span> as a nonresident medical equipment supplier<\/span>. Registration as a nonresident medical equipment supplier<\/span> shall be renewed by March 1 of each year. Applicants for registration or renewal of a registration shall submit a fee specified by the Board<\/span> in regulations at the time of registration or renewal. A nonresident medical equipment supplier<\/span> registered in accordance with this section shall notify the Board<\/span> within 30 days of any substantive change in the information previously submitted to the Board<\/span>. <\/i><\/a><\/p><\/section>\n\t\t\t\t\t\t

B.<\/span> The nonresident medical equipment supplier<\/span> shall at all times maintain a valid, unexpired license, permit, or registration in the state in which it is located, if required by the resident state, and shall furnish proof of such license, permit, or registration upon application for registration or renewal. If the resident state does not require a license, permit, or registration to engage in direct consumer supply of the medical equipment described in subsection A, the applicant shall furnish proof that it meets the minimum statutory and regulatory requirements for medical equipment suppliers<\/span> in the Commonwealth. <\/i><\/a><\/p><\/section>\n\t\t\t\t\t\t

C.<\/span> Records of distribution of medical equipment described in subsection A into the Commonwealth shall be maintained in such a manner that they are readily retrievable from records of distribution into other jurisdictions<\/span> and shall be provided to the Board<\/span>, its authorized agent<\/span>, or any agent<\/span> designated by the Superintendent of State Police upon request within seven days of receipt of such request. <\/i><\/a><\/p><\/section>","plain_text":" CODE OF VIRGINIA\n\nREGISTRATION OF NONRESIDENT MEDICAL EQUIPMENT SUPPLIERS; RENEWAL; FEE (\u00a7\n54.1-3435.3:1)\n\nA. Any person located outside the Commonwealth other than a nonresident pharmacy\nregistered pursuant to § 54.1-3434.1 that ships, mails, or delivers to a\nconsumer in the Commonwealth any hypodermic syringes or needles, medicinal\noxygen, Schedule VI controlled device, those Schedule VI controlled substances\nwith no medicinal properties that are used for the operation and cleaning of\nmedical equipment, sterile water and saline for irrigation, or solutions for\nperitoneal dialysis pursuant to a lawful order of a prescriber shall be\nregistered with the Board as a nonresident medical equipment supplier.\nRegistration as a nonresident medical equipment supplier shall be renewed by\nMarch 1 of each year. Applicants for registration or renewal of a registration\nshall submit a fee specified by the Board in regulations at the time of\nregistration or renewal. A nonresident medical equipment supplier registered in\naccordance with this section shall notify the Board within 30 days of any\nsubstantive change in the information previously submitted to the Board.\n\nB. The nonresident medical equipment supplier shall at all times maintain a\nvalid, unexpired license, permit, or registration in the state in which it is\nlocated, if required by the resident state, and shall furnish proof of such\nlicense, permit, or registration upon application for registration or renewal.\nIf the resident state does not require a license, permit, or registration to\nengage in direct consumer supply of the medical equipment described in\nsubsection A, the applicant shall furnish proof that it meets the minimum\nstatutory and regulatory requirements for medical equipment suppliers in the\nCommonwealth.\n\nC. Records of distribution of medical equipment described in subsection A into\nthe Commonwealth shall be maintained in such a manner that they are readily\nretrievable from records of distribution into other jurisdictions and shall be\nprovided to the Board, its authorized agent, or any agent designated by the\nSuperintendent of State Police upon request within seven days of receipt of such\nrequest.\n\nHISTORY: 2016, c. 88.","edition":{"id":1,"name":"2025","slug":"2025","date_created":"2026-06-21 22:39:22","date_modified":"2026-06-21 22:39:22","current":1,"order_by":1,"last_import":null}}