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How it works

Respimat® re-usable: key features

The patient will need to use this inhaler only once a day. Each time the inhaler is used take two actuations (puffs).

  • If the inhaler has not been used for more than 7 days release one actuation (puff) towards the ground.
  • If the inhaler has not been used for more than 21 days repeat steps 4 to 6 below until a cloud is visible. Then repeat steps 4 to 6 three more times.
respimat inhaler
respimat seperator
Exchangeable cartridge

Exchangeable cartridge and an easy to read dose indicator


Reading the dose indicator

Dose indicator white

The dose indicator shows the number of remaining doses.

Dose indicator yellow

Yellow means there are only 10 or fewer puffs remaining and a new cartridge will soon be needed. 

Dose indicator red

Red tells you when the cartridge is used up and needs replacing. 

respimat seperator

Straightforward assembly


Remove clear base.

  • Keep the cap closed.
  • Press the safety catch while pulling off the clear base with the other hand.
Exchangeable cartridge
Insert new cartridge

Insert new cartridge.

  • Insert the narrow end of the new cartridge into the inhaler
  • Place the inhaler on a firm surface and push down firmly until it clicks into place

Track cartridge.

  • Mark the check-box on the inhaler's label to track the number of cartridges
  • Put the clear base back into place until it snaps back automatically
Track cartridge


  • Keep the cap closed.
  • Turn the clear base in the direction of the arrows on the label until it clicks (half a turn).


  • Open the cap until it snaps fully open.


  • Point the inhaler toward the ground
  • Press the dose-release button.
  • Close the cap.
  • Repeat steps 4-6 until a cloud is visible.
  • After a cloud is visible, repeat steps 4-6 three more times.

Your inhaler is now ready to use and will deliver 60 puffs (30 deses)

respimat seperator

Respimat® re-usable: key features


Exchangeable cartridge and easy to read dose indicator

Dose indicator

Straightforward monthly assembly.
Automatic detachment of clear base when cartridge is empty

Remove clear base
Insert cartridge

Can be reused with up to six cartridges

respimat seperator

Frequently asked questions

  • The patient may have been prescribed a refill cartridge and this should be used together with the inhaler. Each inhaler can be used with up to 6 refill cartridges
  • Not to throw the Respimat® re-usable inhaler away when the cartridge is empty.
  • The cartridge should be replaced when the indicator changes colour to red with a white arrow indicating that the cartridge is empty.
  • To get a new prescription when the dose counter changes colour to yellow

Respimat® re-usable is available as a single pack (one Respimat® re-usable inhaler plus one cartridge) and a single refill pack (one cartridge). One cartridge contains 60 puffs (30 medicinal doses).

Each re-usable inhaler may be used with up to six cartridges, after which time a new Respimat® re-usable inhaler pack should be prescribed.
There is an option within prescribing systems which allows a prescriber to choose refills.

Yes. When designing the Respimat® re-usable, only a few secondary components of the Respimat® inhaler, such as the dose indicator and the length of the body, had to be modified or added. Delivered dose (DD) and particle size distribution (PSD) of the Respimat® re-usable inhaler were compared with data from a disposable Respimat®. Performance, in terms of delivered dose and fine particle dose, was unchanged. The delivered doses over nine cartridges were also stable and consistently within the upper and lower limits of the reference inhaler.

The Respimat® re-usable is licenced for use with up to six cartridges.

Boehringer Ingelheim simplified handling, improved readability of the dose indicator and redesigned the Respimat® for re-use with multiple cartridges based on patient and physician feedback. The Respimat® re-usable also offers the potential to reduce environmental impact from re-use with up to six cartridges.

PC-GB-100906 V1 - October 2020
Adverse events should be reported. Reporting forms and information can be found at Adverse events should also be reported to Boehringer Ingelheim Drug Safety on 0800 328 1627 (Freephone) or
The information on this website has been created by Boehringer Ingelheim. For product information, including patient leaflets and summary of product characteristics, please see Product Information section.
PC-GB-100901 V1 - October 2020