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Health Canada licence record

Licence 105721

SAFESEPT TRANSSEPTAL GUIDEWIRE

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.

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.

FieldValueField name
Licence number105721original_licence_no
Licence statusI (Issued/Active)licence_status
Application risk class2appl_risk_class
Licence nameSAFESEPT TRANSSEPTAL GUIDEWIRElicence_name
Licence name, FrenchSAFESEPT TRANSSEPTAL GUIDEWIRElicence_name_fr
Date of the first issued licence2021-01-13first_licence_status_dt
Date of cancellationnullend_date
Licence typeSingle Devicelicence_type_desc
Company identification number163373company_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.

Company

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.

Devices on this licence

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 IDTrade nameAdded to licenceRemoved
1027914JSONSAFESEPT TRANSSEPTAL GUIDEWIRE2021-01-13null

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.

Decision summaries

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.

ArrHub

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.

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=105721&lang=en&type=json
{
  "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.

Links open the agency’s own records. Unlabelled links open web pages. Links marked (JSON) open an agency’s data record, which a browser shows as plain text.

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