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040 |aCaOODSP|beng|erda|cCaOODSP
043 |an-cn---
0861 |aH164-411/2025E-PDF
24500|aClass III nIVD applications content and classification guidance.
24613|aClass III non-in vitro diagnostic device applications content and classification guidance
264 1|aOttawa, ON : |bHealth Canada = Santé Canada, |cNovember 2025.
264 4|c©2025
300 |a1 online resource (108 pages)
336 |atext|btxt|2rdacontent
337 |acomputer|bc|2rdamedia
338 |aonline resource|bcr|2rdacarrier
500 |aIssued also in French under title: Lignes directrices sur le contenu et la classification des demandes d'homologation d'instruments autres que les instruments diagnostique in vitro de classe III.
500 |a"Pub.: 250339"--Page 2.
504 |aIncludes bibliographical references.
650 0|aMedical instruments and apparatus|xGovernment policy|zCanada.
7101 |aCanada. |bHealth Canada, |eissuing body.
77508|tLignes directrices sur le contenu et la classification des demandes d'homologation d'instruments autres que les instruments diagnostique in vitro de classe III.|w(CaOODSP)9.957369
85640|qPDF|s1.05 MB|uhttps://publications.gc.ca/collections/collection_2026/sc-hc/H164-411-2025-eng.pdf
8564 |qHTML|sN/A|uhttps://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices/application-information/guidance-documents/international-medical-device-regulators-forum/class-iii-nivd-applications-content-classification.html
986 |a250339