Resuscitator, upright, neonate, set

GENERAL DESCRIPTION
Resuscitator intended for full-term babies, preterm and low-weight infants less than 10kg

INTENDED USE
Resuscitators are used for ventilation assistance in critical situations of respiratory distress or failure. It is considered essential equipment for health structures and emergency rescue team (to be available in emergency room, delivery room, operating theatre, intensive care unit, ambulance, etc.).
Guidance and instruction materials have been made available at no cost by the American Academy of Pediatrics via their website:. The Helping Babies Breathe guidance and training materials are freely available in many different languages.

TECHNICAL SPECIFICATIONS
Hand-operated in a vertical position; the inflatable bag is operated an upright position perpendicular to the body being ventilated.
Portable, self-inflating, reusable.
The resuscitator is autoclavable between 121°C and 134°C.
The capacity of the self-inflating ventilation bag is between 220 ml.
The resuscitator has a provision which allows connection of oxygen tubing.
The resuscitator is equipped with a non-rebreather valve.
Resuscitator is easy to disassemble, clean, disinfect, and reassemble.
The resuscitator is equipped with a pressure release (limiting) valve which safeguards against generating ventilation pressures over 45 cmH₂O, while still allowing for an airway pressure of at least 30 cmH₂O.
The pressure release valve should allow to be overridden by the user when higher pressures need to be generated in the airways.
When the pressure release valve is not overridden by the user, it should automatically return to its default position whereby it protects against excess pressures. Users should not be able to lock the pressure release valve in a permanent closed position whereby there is no longer a safeguard against excessive ventilation pressures.
All parts manufactured from high-strength, long-life materials that require no special maintenance or storage conditions.
The resuscitator, all its components and accessories are free of natural rubber latex.
The (intake, non-rebreather) valves are made from polycarbonate/polysulfone or any other material fulfilling ISO 10651-4.
The masks made are of silicone rubber or any material fulfilling ISO 10993-1; ISO 10993-5 or equivalents.
The self-inflating ventilation bag is made of transparent or translucent silicone rubber or any material fulfilling ISO 10651-4 or equivalent.

SUPPLIED WITH
Instructions for assembly, use and maintenance in English, French and Spanish.
1 x Plastic protective pouch which can contain the full set
1 x Mask, transparent: size 0 for preterm and low-weight baby, round type, diameter 35–50 mm
1 x Mask transparent: size 1 for term baby, round type, diameter 50–65 mm

OPTIONAL ACCESSORIES AVAILABLE
At extra costs additional optional features can be requested:
-846151 Oxygen Kit (Complete)
-846156 Newborn mask size 0 Qty 10,
-846157 Newborn mask size 1 Qty 10

ESTIMATED LIFE SPAN
The life span of the device is minimum 3 years or 20 autoclave sessions, whichever comes first.

WARRANTY
Two years from shipping date

ENVIRONMENTAL CONDITIONS
- Operating conditions: -18°C - 45°C / 15% – 90% RH
- Storage conditions: -30°C - 50°C / 40% – 90% RH

WEIGHT AND VOLUME
Weight: 0.28 kg
Volume: 4.59 dm³

ESTIMATED DELIVERY LEAD TIME
65 days

INSTALLATION REQUIREMENTS
The product does not require assembly or commissioning.

TRAINING REQUIREMENTS
User training prior to utilization is recommended.

MAINTENANCE/USER REQUIREMENTS
As per user and service manuals.

RELATED PRODUCTS
S08450151, Resuscitator,hand-oper.,child,set
S0845152, Resuscitator,hand-oper.,adult,set
S0845006, Bulb, suction, neonatal, reusable

ALTERNATIVE PRODUCTS
S0845009, Resuscitator,hand-oper.,neonate,set

COMPONENT OF A KIT
No part of a kit.

QUALITY MANAGEMENT SYSTEM
- Manufacturer is certified for ISO 13485 Medical devices - Quality management systems - Requirements for regulatory purposes.
- Supplier (if not the manufacturer) at a minimum is certified for ISO 9001 Quality management systems – Requirements.

CLASSIFICATION
Classified either under EU MDD 93/42/ECC, or under EU MDR 2017/745 as Class IIa device

SAFETY & PRODUCT STANDARDS
ISO 10651-4 Lung ventilators - Part 4: Lung ventilators -- Part 4: Particular requirements for operator-powered resuscitators (EN 13544-2 implied).
ISO 14971 Medical Devices - Application of Risk Management to Medical Devices
ISO 5356-1 Anaesthetic and respiratory equipment - Conical connectors - Part 1: Cones and sockets
ISO 10993-1 Biological evaluation of medical devices - Part 1: Evaluation and testing
ISO 10993-5 Tests for in vitro cytotoxicity
ISO 15223-1 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements.

NOMENCLATURE
- GMDN code: Pulmonary resuscitator, manual, reusable (17591)
- UMDNS code: Resuscitators, Pulmonary, Manual (13367)