Difference between revisions of "MDCCD Data Warehouse Data Dictionary"

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|Yes
 
|Yes
 
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|February 13, 2024 The company is having the manufacturer of the rescue
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|The inspector sent follow-up letter to address Physio-controls response--the manufacturer can have more than one ID on the label as long as it clearly marks what the device identifier is and that this identifier matches what is in the MDALL. March 6, 2024 The company sent follow-up from manufacturer.  The manufacturer has sent in a fax back to Health Canada to include the device ID (11141-000165) under their license. This adequately addresses the observation.
 
 
kits provide labels.  The manufacturer (Physio Control Inc) of the lifepakbatteries felt that they did not need to address the labelling as theywere under the understanding that as a replacement the battery fell underthe original kit.February 19, 2024 The inspector sent follow-up letter to addressPhysio-controls response--the manufacturer can have more than one ID onthe label as long as it clearly marks what the device identifier is andthat this identifier matches what is in the MDALL.March 6, 2024 The company sent follow-up from manufacturer.  Themanufacturer has sent in a fax back to Health Canada to include the deviceID (11141-000165) under their license. This adequately addresses theobservation
 
 
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Revision as of 16:33, 14 May 2024

Overview

This page provides a data dictionary for each table that is held within the MDCCD Data Warehouse.

Medical Devices

MD_INS_CASE_CAPA

This table holds information about the corrective action plan for an inspection observation.

Column Name Data Type Nullable Data Default Example Data Description
CAPA_ID VARCHAR2(36 CHAR) No NULL ad5e55f6-8b21-ee11-9966-000d3ae86452 This is the unique record identifier for the CAPA.
INSP_ID VARCHAR2(36 CHAR) No NULL 3d7a309e-ce46-40c5-a6c2-f3ea80971d48
INSP_NUM VARCHAR2(200 CHAR) No NULL 00086-BENEMAX DBA. BENEMAX HEALTH AND WELLNESS
OBS_ID VARCHAR2(36 CHAR) No NULL 07244e35-fbf1-ee11-a1fe-6045bd6005cc
CAPA_TYPE VARCHAR2(100 CHAR) Yes NULL Follow Up Plan
CAPA_PLAN VARCHAR2(2000 CHAR) Yes NULL The inspector sent follow-up letter to address Physio-controls response--the manufacturer can have more than one ID on the label as long as it clearly marks what the device identifier is and that this identifier matches what is in the MDALL. March 6, 2024 The company sent follow-up from manufacturer.  The manufacturer has sent in a fax back to Health Canada to include the device ID (11141-000165) under their license. This adequately addresses the observation.
CREATEDBYNAME VARCHAR2(100 CHAR) Yes NULL Jeff Tyndall
CREATEDON DATE Yes NULL 22-08-26
MODIFIEDBYNAME VARCHAR2(100 CHAR) Yes NULL Jeff Tyndall
MODIFIEDON DATE Yes NULL 22-08-26