ページを印刷するundesired operation of the device.
This product is approved in accordance to R&TTE directive transmitter.
Hereby, [iHealth Labs Inc],declares that this BPM1AE is in compliance
with the essential requirements and other relevant provisions of
Directive 1999/5/EC. Directive 1999/5/EC declaration of conformity can
be downloaded on the following link:
https://www.ihealthlabs.eu/support/certifications
Ce produit est conforme à l'Industry Canada. IC: RSS-247
DECLARATION IC
Le présent appareil est conforme aux CNR d'Industrie Canada applicablesaux appareils ra
dio exempts de licence. L'exploitation est autorisée aux deux conditions suivantes :
(1) l'appareil ne doit pas produire de brouillage, et
(2) l'utilisateur de l'appareil doit accepter tout brouillage radioélectrique subi, même si le br
ouillage est susceptible d'en compromettre lefonctionnement.
Ce produit a été approuvé conformément au directives R&TTE de l'émetteur.
Par la présente, [iHealth Labs Inc.] déclare que l'appareil [BPM1AE] est conforme aux
exigences essentielles et aux autres dispositions pertinentes de la directive 1999/5/CE. La
déclaration de conformité, les documents réglementaires et certifications iHealth peuvent
être consultés via ce lien : https://www.ihealthlabs.eu/support/certifications
OTHER STANDARDS AND COMPLIANCES
The Blood Pressure Monitor corresponds to the following standards:
IEC 60601-1:2005 +A1:2012(E)/EN 60601-1：2006/A11: 2011 (Medical
electrical equipment -- Part 1: General requirements for basic safety
and essential performance), IEC 60601-1-2:2014(Medical electrical
equipment -- Part 1-2: General requirements for basic safety and
essential performance - Collateral standard: Electromagnetic
compatibility - Requirements and tests), IEC80601-2-30:2009+AMD1：
2013/EN 80601-2-30:2010/A1：2015(Medical electrical equipment –Part
2-30: Particular requirements for the basic safety and essential
performance of automated non-invasive sphygmomanometers)EN 1060-1:
1995 + A2: 2009 (Non-invasive sphygmomanometers - Part 1: General
requirements), EN 1060-3: 1997 + A2: 2009 (Non-invasive
sphygmomanometers - Part 3: Supplementary requirements for
electro-mechanical blood pressure measuring systems).
ELECTROMAGNETIC COMPATIBILITY INFORMATION
This product is applicable to the equipment and system requirements
for the purpose of receiving radio frequency energy for the purpose
of the work, Wi-Fi receive bandwidth 22M. This product can also be used
to include RF transmitter equipment and system requirements and
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