Amendment device licence application, application 383243
Decision date 2024-12-06. Filed 2024-09-13.
Prints no terms and conditions.
MEDTRONIC INC.
710 Medtronic Parkway N.E.
Minneapolis MN 55432, US
Company status A
Health Canada licence record
Licence 69537
SINGLE AND DUAL CHAMBER RATE RESPONSIVE PACEMAKERS
Medical device licence on Health Canada’s active licence listing (MDALL). Class IV. Status I, which the register defines as Issued/Active. First issued 20 October 2005.
Licence
Each row is one field of the agency record. The grey name beside the label is the field’s name in the agency’s own documentation.
| Field | Value | Field name |
|---|---|---|
| Licence number | 69537 | original_licence_no |
| Licence status | I (Issued/Active) | licence_status |
| Application risk class | 4 | appl_risk_class |
| Licence name | SINGLE AND DUAL CHAMBER RATE RESPONSIVE PACEMAKERS | licence_name |
| Licence name, French | SINGLE AND DUAL CHAMBER RATE RESPONSIVE PACEMAKERS | licence_name_fr |
| Date of the first issued licence | 2005-10-20 | first_licence_status_dt |
| Date of cancellation | null | end_date |
| Licence type | Device Family | licence_type_desc |
| Company identification number | 114663 | company_id |
Source: Health Canada MDALL, licence 69537, API record retrieved 2026-10-10 22:15 Eastern. Status codes as defined in the MDALL API guide.
Company
The licence holder as the register records it. The company page lists every licence under this identification number.
Resolution
No verified alias in ArrHub’s table; the name stands as the register spells it.
Devices on this licence
Each device the register lists under licence 69537, with the date it was added. Later additions do not change the date of the first issued licence.
| Device ID | Trade name | Added to licence | Removed |
|---|---|---|---|
| 217056JSON | ADAPTA DUAL CHAMBER RATE RESPONSIVE PACEMAKER | 2005-10-20 | null |
| 217057JSON | VERSA DUAL CHAMBER RATE RESPONSIVE PACEMAKER | 2005-10-20 | null |
| 217058JSON | SENSIA DUAL CHAMBER RATE RESPONSIVE PACEMAKER | 2005-10-20 | null |
| 588379JSON | ADAPTA SINGLE CHAMBER RATE RESPONSIVE PACEMAKER | 2013-03-25 | null |
| 588380JSON | SENSIA SINGLE CHAMBER RATE RESPONSIVE PACEMAKER | 2013-03-25 | null |
| 1000773JSON | ATTESTA DR MRI SURESCAN | 2018-07-27 | null |
| 1000774JSON | ATTESTA L DR MRI SURESCAN | 2018-07-27 | null |
| 1000775JSON | ATTESTA S DR MRI SURESCAN | 2018-07-27 | null |
| 1000776JSON | ATTESTA SR MRI SURESCAN | 2018-07-27 | null |
| 1000777JSON | SPHERA DR MRI SURESCAN | 2018-07-27 | null |
| 1000778JSON | SPHERA L DR MRI SURESCAN | 2018-07-27 | null |
| 1000779JSON | SPHERA SR MRI SURESCAN | 2018-07-27 | null |
Source: Health Canada MDALL, device records for licence 69537, retrieved 2026-10-10 22:15 Eastern. Device identifiers link to the agency’s device record.
Decision summaries
Regulatory Decision Summaries Health Canada has published for this licence, newest first. Each links to the agency’s record.
Amendment device licence application, application 351203
Decision date 2023-05-02. Filed 2022-08-23.
Prints no terms and conditions.
Source: Health Canada, Drug and Health Product Register, Regulatory Decision Summaries, retrieved 2026-10-10 22:15 Eastern. Terms and conditions as the summary prints them.
ArrHub
What ArrHub adds to the record. Everything above this line is the agency’s; everything here is ArrHub’s, dated and attributed.
Electrophysiology
Confirmed by review, before 24 September 2026; the review record carries no timestamp.
Record pair
No confirmed pair across the two registers for this record.
First seen by ArrHub’s weekly snapshot: 2026-09-20 09:05 Eastern.
Raw record
The stored record exactly as ArrHub holds it, for anyone who wants to check the page against it.
Show the raw record (JSON)api/medical-devices/licence/?id=69537&lang=en&type=json
{
"original_licence_no": 69537,
"licence_status": "I",
"licence_status_desc": "Issued/Active",
"appl_risk_class": 4,
"licence_name": "SINGLE AND DUAL CHAMBER RATE RESPONSIVE PACEMAKERS",
"licence_name_fr": "SINGLE AND DUAL CHAMBER RATE RESPONSIVE PACEMAKERS",
"first_licence_status_dt": "2005-10-20",
"end_date": null,
"licence_type_desc": "Device Family",
"company_id": 114663,
"company_name": "MEDTRONIC INC.",
"country_cd": "US",
"city": "Minneapolis",
"source_url": "https://health-products.canada.ca/api/medical-devices/licence/?id=69537&lang=en&type=json",
"verified_at": "2026-09-20T02:17:28.644842+00:00",
"ep_confirmed_at": null,
"collected_at": "2026-10-11T02:15:33.877+00:00",
"last_checked_at": "2026-10-11T02:15:33.877+00:00",
"record_url": "https://health-products.canada.ca/mdall-limh/information?licenceId=69537&type=active&lang=eng",
"company_record_url": "https://health-products.canada.ca/mdall-limh/information?companyId=114663&lang=eng"
}The readable page is rendered from the record held in ArrHub’s verified view; the agency record at health-products.canada.ca governs where they differ.
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