PRESSURE PRODUCTS MEDICAL DEVICE MANUFACTURING LLC
1 School Street
Morton PA 19070, US
Company status A
Health Canada licence record
Licence 105721
Medical device licence on Health Canada’s active licence listing (MDALL). Class II. Status I, which the register defines as Issued/Active. First issued 13 January 2021.
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 | 105721 | original_licence_no |
| Licence status | I (Issued/Active) | licence_status |
| Application risk class | 2 | appl_risk_class |
| Licence name | SAFESEPT TRANSSEPTAL GUIDEWIRE | licence_name |
| Licence name, French | SAFESEPT TRANSSEPTAL GUIDEWIRE | licence_name_fr |
| Date of the first issued licence | 2021-01-13 | first_licence_status_dt |
| Date of cancellation | null | end_date |
| Licence type | Single Device | licence_type_desc |
| Company identification number | 163373 | company_id |
Source: Health Canada MDALL, licence 105721, API record retrieved 2026-10-17 22:15 Eastern. Status codes as defined in the MDALL API guide.
The licence holder as the register records it. The company page lists every licence under this identification number.
PRESSURE PRODUCTS MEDICAL DEVICE MANUFACTURING LLC
1 School Street
Morton PA 19070, US
Company status A
Resolution
No verified alias in ArrHub’s table; the name stands as the register spells it.
Each device the register lists under licence 105721, 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 |
|---|---|---|---|
| 1027914JSON | SAFESEPT TRANSSEPTAL GUIDEWIRE | 2021-01-13 | null |
Source: Health Canada MDALL, device records for licence 105721, retrieved 2026-10-17 22:15 Eastern. Device identifiers link to the agency’s device record.
Regulatory Decision Summaries Health Canada has published for this licence, newest first. Each links to the agency’s record.
No regulatory decision summary is held for this licence.
Source: Health Canada, Drug and Health Product Register, Regulatory Decision Summaries, retrieved 2026-10-17 22:15 Eastern. Terms and conditions as the summary prints them.
What ArrHub adds to the record. Everything above this line is the agency’s; everything here is ArrHub’s, dated and attributed.
Electrophysiology
Classified against the published categories, 18 October 2026.
First seen by ArrHub’s weekly snapshot: 2026-09-20 09:05 Eastern.
The stored record exactly as ArrHub holds it, for anyone who wants to check the page against it.
{
"original_licence_no": 105721,
"licence_status": "I",
"licence_status_desc": "Issued/Active",
"appl_risk_class": 2,
"licence_name": "SAFESEPT TRANSSEPTAL GUIDEWIRE",
"licence_name_fr": "SAFESEPT TRANSSEPTAL GUIDEWIRE",
"first_licence_status_dt": "2021-01-13",
"end_date": null,
"licence_type_desc": "Single Device",
"company_id": 163373,
"company_name": "PRESSURE PRODUCTS MEDICAL DEVICE MANUFACTURING LLC",
"country_cd": "US",
"city": "Morton",
"source_url": "https://health-products.canada.ca/api/medical-devices/licence/?id=105721&lang=en&type=json",
"verified_at": "2026-09-20T02:17:33.738227+00:00",
"ep_confirmed_at": "2026-10-18T00:00:00+00:00",
"collected_at": "2026-10-18T02:15:32.83+00:00",
"last_checked_at": "2026-10-18T02:15:32.83+00:00",
"record_url": "https://health-products.canada.ca/mdall-limh/information?licenceId=105721&type=active&lang=eng",
"company_record_url": "https://health-products.canada.ca/mdall-limh/information?companyId=163373&lang=eng",
"ep_confirmed_method": "rule"
}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.
Contains information licensed under the Open Government Licence – Canada.
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