Pure Global AI
Health Canada SOR

SOR/98-282 Schedule 1 Part 2

In Vitro Diagnostic Device Classification
CanadaHealth CanadaClassificationEffective July 1, 1998
Official source linked
What this code is

SOR/98-282 Schedule 1 Part 2 is the official HC identifier for “In Vitro Diagnostic Device Classification”. SOR/98-282 Schedule 1 Part 2 is the official identifier HC uses for this instrument.

Instrument
SOR
Full name
SOR/98-282 Schedule 1 Part 2
Category
Classification
Source links
Authority source
English
Open the issuing-authority text
Issuing-authority publication; confirm whether a later amendment or consolidated version applies.
Readable HTML
Section view of SOR/98-282
Open this passage in the parent instrument →
This metadata row is a virtual view. The official text is ingested once as SOR/98-282.
Dates
Published
—
Effective
July 1, 1998
Consolidated through
2026-06-17
Readable full text

Open a language version

Each version has stable passage anchors for direct citations and highlighting. The readable text is generated from an authority source and does not replace the legally controlling publication.

English full text196 articles · English — official textRead HTML →French full text196 articles · French — official textRead HTML →
About this regulation

In Vitro Diagnostic Device Classification

Section view of Schedule 1 Part 2 IVD classification rules. Official Schedule 2 is “Implants”; the previous Schedule 2 IVD label was corrected against the Justice Laws consolidated text.

SOR/98-282 Schedule 1 Part 2 is the official identifier HC uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.

Verified