Medical Devices Regulations (SOR/98-282)

Regulations are current to 2012-05-14 and last amended on 2011-12-16. Previous Versions

SCHEDULE 3

(Section 89)

EXPORT CERTIFICATE FOR MEDICAL DEVICES

UNDER THE Medical Devices Regulations

I, , certify that I have knowledge of all matters contained in this certificate and that

  • 1. I am (check applicable box)

    • (a) where the medical device described in this certificate is exported by a corporation

      • ☐ 
        the exporter’s senior executive officer,
      • ☐ 
        the exporter’s senior regulatory officer,
      • ☐ 
        the authorized agent of the exporter’s senior executive officer, or
      • ☐ 
        the authorized agent of the exporter’s senior regulatory officer; and
    • (b) where the medical device described in this certificate is exported by an individual

      • ☐ 
        the exporter, or
      • ☐ 
        the exporter’s authorized agent.

__________

, (State name and address of exporter or, if a corporation, name and address of principal place of business in Canada).

  • 2. On the day of , , a package containing (description of device, including serial number, model name, lot number and quantity, as applicable; if additional space required, attach as Appendix “A”) is/will be consigned to (name and address of consignee).

  • 3. The package is marked in distinct overprinting with the word “Export” or “Exportation”.

  • 4. The medical device was not manufactured for consumption in Canada.

  • 5. The medical device is not sold for consumption in Canada.

  • 6. The package and its contents do not contravene any known requirement of the law of the country of (state country of consignee).

  • 7. All relevant information is contained in this certificate and no relevant information has been knowingly withheld.

__________

Signature

__________

Position title

,

Date