QWP-CDRRHR/LRD-05 Annex 02

Rev. No. 06 Date Effective: 10 February 2020

CHECKLIST OF REQUIREMENTS FOR CERTIFICATE OF

EXEMPTION FOR PRODUCT REGISTRATION

1. Letter of Intent regarding exemption of the device/product from registration

2. Photocopy of Product Brochure (s)
3. License to Operate as Medical Device Distributor/Importer/Exporter
4. Fee (computation of fee is per product as indicated in the letter of intent)