ApprovalTrail

Medical device licence · 91832 · Class 2

DMEM, DULBECCO'S MODIFIED EAGLE MEDIUM

No longer licensed: discontinued at renewal

Licence status Discontinued at renewal; first licensed August 15, 2013; ended December 1, 2021. It is in Health Canada’s archive of licences no longer in force.
Licence number
91832
Licence holder
Life Technologies Corporation Also Trading As: InvitrogenGrand Island, NY, United States
Risk class
Class II (low to moderate risk)
Licence type
Device Family
First licensed
August 15, 2013
Ended
December 1, 2021
Devices covered
10

Devices on this licence

By name, as listed. The official record lists model numbers and identifiers.

  • DMEM, DULBECCO'S MODIFIED EAGLE MEDIUM (HIGH GLUCOSE)
  • DMEM, DULBECCO'S MODIFIED EAGLE MEDIUM (HIGH GLUCOSE, GLUTAMAX)
  • DMEM, DULBECCO'S MODIFIED EAGLE MEDIUM (HIGH GLUCOSE, GLUTAMAX, HEPES)
  • DMEM, DULBECCO'S MODIFIED EAGLE MEDIUM (HIGH GLUCOSE, HEPES)
  • DMEM, DULBECCO'S MODIFIED EAGLE MEDIUM (HIGH GLUCOSE, NO GLUTAMINE)
  • DMEM, DULBECCO'S MODIFIED EAGLE MEDIUM (HIGH GLUCOSE, PYRUVATE)
  • DMEM, DULBECCO'S MODIFIED EAGLE MEDIUM (HIGH GLUCOSE, PYRUVATE, NO GLUTAMINE)
  • DMEM, DULBECCO'S MODIFIED EAGLE MEDIUM (LOW GLUCOSE, GLUTAMAX, PYRUVATE)
  • DMEM, DULBECCO'S MODIFIED EAGLE MEDIUM (LOW GLUCOSE, PYRUVATE)
  • DMEM, DULBECCO'S MODIFIED EAGLE MEDIUM (LOW GLUCOSE, PYRUVATE, HEPES)

Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.