Medical device licence · 90042 · Class 2
GLIDESHEATH SLENDER
No longer licensed: discontinued at renewal
Licence status Discontinued at renewal; first licensed November 5, 2012; ended October 14, 2020. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 90042
- Licence holder
- Terumo CorporationTokyo, --, Japan
- Risk class
- Class II (low to moderate risk)
- Licence type
- Device Group Family
- First licensed
- November 5, 2012
- Ended
- October 14, 2020
- Devices covered
- 1
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- GLIDESHEATH SLENDER HYDROPHILIC COATED INTRODUCER SHEATH
Recalls and safety alerts that mention it
Health Canada’s recall notices do not carry licence numbers, so these are matched by name: notices whose title or product names “glidesheath”. A notice may cover another product or only some lots: read it to see what it covers.
- Glidesheath Slender® Introducer SheathJuly 2, 2026 · Cardiovascular · Performance · Type II
- Glidesheath Slender Hydrophilic Coated Introducer SheathJune 13, 2017 · Medical devices · Type II
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.