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Optiflow Junior 2 Blender Transition Kit Mr850

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535 views2 pages

Optiflow Junior 2 Blender Transition Kit Mr850

Uploaded by

jacp.1190
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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Blender Transition Kits

SPECIFICATIONS

PRODUCT OJR410B OJR412B OJR414B OJR416B OJR418B


NASAL CANNULA SIZE XS S M L XL
Description F&P Optiflow™ F&P Optiflow™ F&P Optiflow™ F&P Optiflow™ F&P Optiflow™
Junior 2 Blender Junior 2 Blender Junior 2 Blender Junior 2 Blender Junior 2 Blender
Transition Kit – XS Transition Kit – S Transition Kit – M Transition Kit – L Transition Kit – XL

Weight (per kit) 31.2 g 31.6 g 33.8 g 38 g 38.3 g

FLOW RATES* (L/min) - MR850


BC151
BC161
4-8 4-9 4-10 4-15 4-15
BC153
BC163

COMPATIBLE SPARES

F&P Wigglepad™ 2
WJR110 WJR112

PRODUCT SPECIFICATIONS
Compatible circuits BC151, BC161, BC153, BC163
Connection Easy-click connector, adaptor
Compatible humidifier MR850 (in invasive mode)
Quantity Box of 5
Box components F&P Optiflow Junior nasal cannula, proprietary adaptor, OJR215 pressure relief manifold, user instructions

* Flow rates above describe technical capability of the product when used at sea level.
Ensure clinical judgement is used when prescribing flow rates.

www.fphcare.com
Blender Transition Kits | SPECIFICATIONS

PERFORMANCE SPECIFICATIONS
Ambient range 18-26 °C / 64-79 °F

Usage Single patient use

Duration of use 7 days

Recommended gas source Medical gas

Shelf life 3 years

Nominal relief pressure 40 cmH2O

COMPONENTS AND COMPOSITION


Cannula predominant materials Thermoplastic Elastomer; Hydrocolloid; ABS; Stainless steel

Adaptor predominant materials Polypropylene

Manifold predominant materials Thermoplastic Elastomer White; ABS; Stainless steel; Silicon rubber

Materials not present Not manufactured with natural rubber latex, PVC or Phthalates (DEHP, DBP, BBP)

Manufacturing mode Produced in a controlled working environment

Incineration or according to hospital protocol for cannula, manifold and adapter;


Disposal
Clamshell packaging and label recyclable PET

REGULATORY
Classification AU-IIa, EU-IIa, Canada-II, US-II

Country of origin New Zealand

Notified body TÜV SÜD Product Services GmbH CE0123

Standard Medical tapers used comply with ISO 5356-1


PM-612906 REV A © 2017 Fisher & Paykel Healthcare Limited

Please note that the information in this specifications sheet (including product information and images) is summarized and provided for illustrative purposes only.
Please refer to the relevant user instructions for more information and confirm details with your local Fisher & Paykel Healthcare representative prior to placing an
order. Information subject to change without notice.

www.fphcare.com

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