Medical device licence · 27606 · Class 2
VACUETTE MULTI-DRAWING NEEDLE
No longer licensed: cancelled: quality-system requirement (2003)
Licence status Cancelled: quality-system requirement (2003); first licensed February 20, 2001; ended February 16, 2004. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 27606
- Licence holder
- Greiner Bio One GmbhKremsmuenster, Austria
- Risk class
- Class II (low to moderate risk)
- Licence type
- Single Device
- First licensed
- February 20, 2001
- Ended
- February 16, 2004
- Devices covered
- 1
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- VACUETTE MULTI-DRAWING NEEDLE
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 “vacuette”. A notice may cover another product or only some lots: read it to see what it covers.
- VACUETTE® 2 mL 9NC Coagulation Sodium Citrate 3.2%November 5, 2025 · General hospital and personal use · Labelling and packaging · Type II
- VACUETTE® Sample Transfer UnitJanuary 7, 2025 · General hospital and personal use · Performance · Type II
- Vacuette 4 Ml Fx Sodium Fluoride / Potassium Oxalate TubeJanuary 9, 2024 · Medical devices · Performance · Type II
- Vacuette® Tube 5 mL Cat Serum Separator Clot ActivatorMay 25, 2023 · General hospital and personal use · Performance · Type II
- Vacuette * K2 EDTAMarch 23, 2023 · General hospital and personal use · Performance · Type II
- VACUETTE 2 ml K2 EDTA (2021-09-17)October 22, 2021 · Medical devices · Medical devices · Type II
- Vacuette 4 mL FX Sodium/Fluoride /Potassium oxalSeptember 23, 2016 · Medical devices · Type II
- VACUETTE 4 ML FX SODIUM FLUORIDE / POTASSIUM OXAL (2016-04-26)May 31, 2016 · 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.