Free shipping in Germany• Delivery time: 1–3 business days

Why
LifeSaveAir®?

Because it’s all in the details.
In the technology. In the manufacturing. In the documentation.

LifeSaveAir with red handle, white housing and transparent mask
Protection against
Overpressure
A valve prevents overpressure towards the airways.
Limited
Vacuum
The second valve automatically limits the negative pressure.

The application.
Apply. Pull.

This is how the first suction stroke begins – simplified.

LifeSaveAir®

Apply. Pull.

With pre-mounted mask and inserted piston.

  1. Mounting & sealing

    Mounting & sealing

    Hold the mask over the mouth and nose.

  2. Pull out the piston

    Pull out the piston

    Pull straight back until it stops; hold the mask in place.

Overpressure protection Automatic vacuum limitation
LifeSaveAir product detail with round German flag

Made in Germany.
From Development
up to production.

LifeSaveAir® is developed and manufactured in Germany. The product is backed by Jespira GmbH in Dortmund.

German development and production
LifeSaveAir® is developed and manufactured in Germany.
Internal quality controls
Production is subject to internal quality controls.
Local supply chains
During production, we deliberately rely on local supply chains.

Medical device Class I.
Verifiably documented.

LifeSaveAir® is a Class I medical device according to the European Medical Device Regulation (EU) 2017/745.

With the EU Declaration of Conformity, Jespira GmbH declares as the manufacturer under its own responsibility that the listed products meet the applicable requirements.

The declaration identifies the products, their intended purpose, the risk class and the manufacturer responsible.

EU Declaration of Conformity for LifeSaveAir and LifeSaveAir in Case, September 11, 2026 EU Declaration of Conformity · 11.09.2026

In a nutshell.

Why are there two valves?

Because they perform different functions: One valve prevents overpressure toward the airways. The other automatically limits the generated negative pressure to a defined range.

What does Class I medical device mean?

Class I designates the risk class of the medical device. In the EU declaration of conformity for LifeSaveAir®, Class I and classification rule 1 are specified. In it, the manufacturer declares conformity with Regulation (EU) 2017/745.

Does LifeSaveAir® replace first aid?

No. LifeSaveAir® is a complementary aid for acute airway obstructions caused by solid foreign bodies when standard procedures have been unsuccessfully attempted or cannot be performed. The intended use and instructions for use are decisive. In an emergency, immediately call 112 and provide first aid.

Get to know the product.

The device, the three mask sizes, and the scope of delivery.

To LifeSaveAir®