Amendment device licence application, application 402152
Decision date 2025-12-15. Filed 2025-09-22.
Prints no terms and conditions.
MEDTRONIC INC.
710 Medtronic Parkway N.E.
Minneapolis MN 55432, US
Company status A
Health Canada licence record
Licence 110572
PULSESELECT PULSED FIELD ABLATION SYSTEM
Medical device licence on Health Canada’s active licence listing (MDALL). Class IV. Status D, which the register defines as Issued/Conditional. First issued 13 December 2023.
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 | 110572 | original_licence_no |
| Licence status | D (Issued/Conditional) | licence_status |
| Application risk class | 4 | appl_risk_class |
| Licence name | PULSESELECT PULSED FIELD ABLATION SYSTEM | licence_name |
| Licence name, French | PULSESELECT PULSED FIELD ABLATION SYSTEM | licence_name_fr |
| Date of the first issued licence | 2023-12-13 | first_licence_status_dt |
| Date of cancellation | null | end_date |
| Licence type | System | licence_type_desc |
| Company identification number | 114663 | company_id |
Source: Health Canada MDALL, licence 110572, 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 110572, 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 |
|---|---|---|---|
| 1056245JSON | PULSESELECT PULSED FIELD ABLATION LOOP CATHETER | 2023-12-13 | null |
| 1056246JSON | PULSESELECT PULSED FIELD ABLATION GENERATOR | 2023-12-13 | null |
| 1056247JSON | PULSESELECT PULSED FIELD ABLATION REMOTE CONTROL | 2023-12-13 | null |
| 1056248JSON | PULSESELECT PULSED FIELD ABLATION CATHETER INTERFACE CABLE | 2023-12-13 | null |
| 1056249JSON | PULSESELECT PULSED FIELD ABLATION ELECTROGRAM CABLE | 2023-12-13 | null |
| 1056250JSON | PULSESELECT PULSED FIELD ABLATION FOOT SWITCH | 2023-12-13 | null |
Source: Health Canada MDALL, device records for licence 110572, 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 389707
Decision date 2025-01-20. Filed 2024-12-20.
Prints no terms and conditions.
New device licence application, application 365927
Decision date 2023-12-13. Filed 2023-08-03.
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.
FDA record pair
P230017PMA original, product code QZI. FDA decision 13 December 2023. Pair confirmed under the verification protocol by product name, human review, 24 September 2026; reference class pfa_system.
0
Both agency dates fall on the same day.
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=110572&lang=en&type=json
{
"original_licence_no": 110572,
"licence_status": "D",
"licence_status_desc": "Issued/Conditional",
"appl_risk_class": 4,
"licence_name": "PULSESELECT PULSED FIELD ABLATION SYSTEM",
"licence_name_fr": "PULSESELECT PULSED FIELD ABLATION SYSTEM",
"first_licence_status_dt": "2023-12-13",
"end_date": null,
"licence_type_desc": "System",
"company_id": 114663,
"company_name": "MEDTRONIC INC.",
"country_cd": "US",
"city": "Minneapolis",
"source_url": "https://health-products.canada.ca/api/medical-devices/licence/?id=110572&lang=en&type=json",
"verified_at": "2026-09-20T02:17:28.426833+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=110572&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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