Laerdal Silicone Resuscitator (LSR)

All versions

• Easy assembly
• Standard 15/22mm connectors
• HMEF filters with a 15M/22F connector will fit on the LSR
• Designed to prevent rebreathing of exhaled air
• 35cm H² 0 Pressure Relief Valve reduces risk of excessive ventilation pressure
• Long product life
• Can be high-level disinfected and sterilized
• Efficient integrated Intake/Reservoir Valve with reservoir bag ensures oxygen economy and increased oxygen concentration
• Foldable for compact storage to save space
• Available in three packaging configurations: carton, compact case and display case
• Easy decontamination minimizes cleaning time and reduces inventory needs
• Can be reused for years (with proper care)

Temperature and Environment
Operating Temperature Humidity -18˚C to 60˚C (0˚F to 140˚F) 15% to 95% rH
Long term Storage Temperature Humidity 40˚C to 70˚C (-40˚F to 158˚F) 40% to 95% rH

Adult model
Ventilation Bag volume 1600 ml
Reservoir Bag volume 2600 ml
Attainable delivery volume approximately 800 ml

Pediatric model
Ventilation Bag volume 500 ml
Reservoir Bag volume 600 ml
Attainable delivery volume approximately 320 ml

Preterm model
Ventilation Bag volume 240 ml
Reservoir Bag volume 600 ml
Attainable delivery volume approximately 150 ml

Laerdal Silicone Resuscitator meets the following Standards:
EN 1789
ISO 10651-4
ISO 13485
ISO 14971
ISO 5356-1
ISO 10993-1

Europe: CE marked as Class IIa device in accordance with Council Directive 93/42/EEC Medical Device Directive, as amended by Council Directive 2007/47/EC.

USA: Cleared under 510(k) as a class 2 device.

Canada: Holds a class 2 medical device license.

The Laerdal Silicone Resuscitator is available in three sizes; adult, pediatric and pre-term.

The Adult model is intended for patients over 25 kg (55 lb.).
The Pediatric model is intended for patients from 2.5 kg (5.5 lb.) to 25 kg (55 lb.).
The Preterm model is intended for patients below 2.5 kg (5.5 lb.).

Technical service is not available for the Laerdal Silicone Resuscitator