Medical device discontinuation: Fetal Spiral Electrode
The Fetal Spiral Electrode is reported as a medical device discontinuation under subsection 62.23(2) of the Medical Devices Regulations. Updates to the status of a discontinuation can be found on the List of shortages and discontinuations webpage.
Posted on [2023-04-20]Footnote 1
Type of report
Discontinuation
Discontinuation status
Discontinued
Name of medical device (including any component, accessory or part that is discontinued, including the model name) if applicable
Fetal Spiral Electrode
Other names (for example, trade name), if applicable
n/a
Package description (for example, packaging formats, sizes, quantities)
Box of 25
Class of medical device (I, II, III or IV), if known
Class II
Device identifier(s) (for example, serial number, catalogue number, part number, model number or unique device identifier)
9898 031 37631
Medical device licence number (for Class II, III and IV), if applicable
14018
Authorization identification number (for devices authorized for importation or sale under an interim order made under section 30.1 of the Food and Drugs Act), if applicable
n/a
Single-use product
Yes
Importers that have reported the discontinuation (names of importers listed who have reported the discontinuation separately from the manufacturer or who are reporting on behalf of the manufacturer in a delegated capacity), if applicable
n/a
Manufacturer's name
Philips Medical Systems
Manufacturer's mailing address
3000 Minuteman Road
Andover, Massachusetts
USA
01810-1099
Reason for discontinuation
Business reasons
Comments
n/a
Footnotes
- Footnote 1
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This date reflects when a discontinuation report is first posted online. This page includes specific information related to the device that is being discontinued. Updates to the status of a discontinuation can be found on the List of shortages and discontinuations webpage.
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