PhiLaser Type 2.0
Brand(s)
Last updated
Summary
Product
PhiLaser Type 2.0
Issue
Medical devices - Unauthorised device
What to do
Contact the manufacturer if you require additional information.
Audience
Industry
Affected products
Affected products |
Lot or serial number |
Model or catalog number |
|---|---|---|
PhiLaser Type 2.0 |
All lots. |
R 2.0 |
Issue
Health Canada advised that the Philaser Type 2.0 device is considered a class III medical device and requires a licence. The Philaser Type 2.0 device is not currently licensed, so we have stopped sales and advertisement of the Philaser Type 2.0 device in Canada as of March 20, 2023.
Recall start date: May 19, 2023
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General and plastic surgery
Companies
Phiacademy Gmbh
Gartengasse 8/8, 1050, Vienna, Austria
Published by
Health Canada
Audience
Industry
Recall class
Type II
Identification number
RA-73735
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