Medical device licence · 84738 · Class 3
NUCLISENS LYSIS BUFFER
No longer licensed: discontinued at renewal
Licence status Discontinued at renewal; first licensed December 15, 2010; ended October 28, 2019. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 84738
- Licence holder
- Biomerieux SaRockland, MA, United States
- Risk class
- Class III (moderate to high risk)
- Licence type
- Single Device
- First licensed
- December 15, 2010
- Ended
- October 28, 2019
- Devices covered
- 1
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- NUCLISENS LYSIS BUFFER
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 “nuclisens”. A notice may cover another product or only some lots: read it to see what it covers.
- Nuclisens® - Magnetic SilicaJuly 11, 2022 · Medical devices · Performance · Type II
- NucliSENS Lysis Buffer (2020-01-14)February 7, 2020 · Medical devices · Medical devices · Type II
- NUCLISENS LYSIS BUFFER (2017-07-13)October 30, 2017 · Medical devices · Medical devices · Type II
- Nuclisens Easymag - Magnetic SilicaJanuary 25, 2017 · Medical devices · Medical devices · Type II
- NucliSENS Magnetic Silica and Extraction Reagents (2016-11-23)November 30, 2016 · Medical devices · Medical devices · Type I
- NUCLISENS EASYMAG - MAGNETIC SILICA (2016-07-08)July 19, 2016 · Medical devices · Medical devices · Type I
- NucliSENS Easymag Lysis Buffer (2014-03-06)April 4, 2014 · Medical devices · Medical devices · Type II
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.