(A) The director shall provide a data collection tool for the review of child deaths or arrange for the use of a national child death review database. The individual data collected shall be maintained in a confidential manner.
(B) Each CFR board shall use the director's data collection tool or the national child death review database to record the following information:
(1) Demographic information that includes:
(a) Age of the child
(b) Sex of the child, identified as male or female;
(c) Race of the child, identified as black, white, native American, Asian, Alaskan native, native Hawaiian, Pacific islander, unknown or multiple; and
(d) Ethnicity of the child, identified as Hispanic or Latino origin.
(2) Death related information, that includes:
(a) Year of child's death;
(b) Geographic location of death;
(c) Cause of death; and
(d) Contributing factors to death.
(3) Any other information the CFR board considers relevant to the review.
(C) Individual data related to a child death review that is reported on the data collection tool or the national child death review database is not a public record under section 149.43 of the Revised Code.