
AnaConDa-S is an enhancement of AnaConDa and is designed in a way that enables many more patients, including those with lower lung capacity, to be sedated, which was not possible with the older model. AnaConDa-S expands the target group by around 25 per cent, and the response from the health service has been very positive. Sedana Medical anticipates that AnaCon-Da will gradually replace the old AnaConDa model.
The development work has been successfully carried out by Sedana Medical’s Development Department in Ireland, headed by Ron Farrell, COO/R&D. AnaConDa-S gained approval and a CE mark in Europe on 16 January 2017 and Germany will be first country in which it is launched in March 2017.
“The development of a new generation of AnaConDa goes hand-in-hand with our ongoing efforts with a clinical study, which is intended to lead to marketing authorisation for our pharmaceutical IsoConDa® (isoflurane) for inhalation sedation in intensive care, and the expansion of our sales organisation. Since the start of the year, we have taken a major step towards realising our vision of making inhalation sedation with IsoConDa and AnaConDa a global standard method for the sedation of mechanically ventilated patients in intensive care,” says Christer Ahlberg, CEO of Sedana Medical AB (publ).
For further information, contact:
Christer Ahlberg, CEO Sedana Medical AB (publ)
Mobile: +46 (0)70 – 675 33 30, Email: christer.ahlberg@sedanamedical.com