Claris Healthcare Reflex Petunjuk Penggunaan Manual - Halaman 4
Jelajahi secara online atau unduh pdf Petunjuk Penggunaan Manual untuk Peralatan Medis Claris Healthcare Reflex. Claris Healthcare Reflex 6 halaman. Knee rehabilitation system
Halaman CetakWARNINGS & SAFETY PRECAUTIONS
Read all the information in this Guide and other
provided instructions before operating the system.
Do not expose sensor to water. Remove sensor prior to
bathing, showering, or swimming.
Do not attempt to disassemble or change the battery.
This device meets FCC and IC regulations if used as
specified. See last page for details.
Consult your physician for any of the following
situations:
a. Allergic reaction to the adhesive pads including any skin
redness or inflammation
b. Simultaneous use with other medical monitoring or bracing
equipment on the same limb
USING YOUR CLARIS REFLEX SYSTEM
1. Read through and follow the
Claris Reflex tablet.
2. Familiarize yourself with the Exploring your Claris Reflex
Screen Guide
.
3. When it's time, your tablet will automatically prompt you to
attach your sensor to the side of your knee. At that time, follow
When it's Time to Attach your Sensor
the
4. You can review the above information and other instructional
videos at any time by pressing the
Claris Reflex tablet screen.
5. If you have any trouble with your Claris Reflex, please review
the TROUBLESHOOTING FAQs section below or see the
CONTACT INFORMATION section above.
800-004-01-90 | Claris Healthcare | 1-844-369-9977 ext2 | [email protected] | Page 3
Quick Start Guide
to power on your
instructions.
Resources
button on your
PRODUCT SPECIFICATIONS
FCC Part 15
This device complies with FCC Rules Part 15 operation is subject to the following two
conditions:
1. This device may not cause harmful interference.
2. This device must accept any interference, including interference that may cause
undesired operation of the device.
Changes or modifications to this device, not expressly approved by Claris, could void
the user's authority to operate the equipment.
2AOOK-REFLEX1
Industry Canada Notifications
This device complies with Industry Canada's license-exempt RSSs. Operation is
subject to the following two conditions:
(1) This device may not cause interference; and
(2) This device must accept any interference, including interference that may cause
undesired operation of the device.
Le présent appareil est conforme aux CNR d'Industrie Canada applicables aux
appareils radio exempts de licence. L'exploitation est autorisée aux deux conditions
suivantes:
(1) l'appareil ne doit pas produire de brouillage;
(2) l'utilisateur de l'appareil doit accepter tout brouillage radioélectrique subi, même si
le brouillage est susceptible d'en compromettre le fonctionnement.
IC: 23491-REFLEX1
800-004-01-90 | Claris Healthcare | 1-844-369-9977 ext2 | [email protected] | Page 8