Otsuka America Pharmaceutical 06120 Proteus Patch, Model SPC-0800 User Manual2

Download:
Mirror Download [FCC.gov]
Document ID	2179624
Application ID	mW7HFgzbB13Edqh709jiFw==
Document Description	Users Manual2
Short Term Confidential	No
Permanent Confidential	No
Supercede	No
Document Type	User Manual
Display Format	Adobe Acrobat PDF - pdf
Filesize	20.46kB (255799 bits)
Date Submitted	2014-01-28 00:00:00
Date Available	2014-01-28 00:00:00
Creation Date	2014-01-14 15:59:54
Producing Software	Acrobat Distiller 10.1.8 (Windows)
Document Lastmod	2014-01-14 15:59:54
Document Title	Microsoft Word - LBL-0176 Rev 1 DW5 Patch User Supplemental Information.docx
Document Creator	PScript5.dll Version 5.2.2
Document Author:	jhutchison

THE PROTEUS PATCH
SPC‐0800
USER SUPPLEMENTAL INFORMATION
Table of Contents
1. TECHNICAL INFORMATION ................................................................................................................ 2
1.1 – Classification .................................................................................................................................... 2
1.2 – Environmental Conditions .......................................................................................................... 2
1.3 – Minimizing Skin Irritation ............................................................................................................ 2
1.4 – Protection against Ingress of Solids and Liquids ................................................................. 2
1.5 – Avoiding Unsafe Use Conditions .............................................................................................. 2
1.6 – Information on Electromagnetic and Other Interferences............................................... 3
1.7 – Information on the Radio Subsystem ...................................................................................... 3
1.8 – European R&TTE Declaration of Conformity ......................................................................... 7
1.9 – CISPR Interference Statement .................................................................................................... 7
1.10 – FCC Interference Statement ..................................................................................................... 8
1.11 – FCC Wireless Notice..................................................................................................................... 8
1.12 – FCC Identifier ................................................................................................................................. 8
2 – DISPOSAL OF WASTE PRODUCTS .................................................................................................. 8
3 – MANUFACTURER CONTACT INFORMATION ............................................................................. 9
LBL‐0176, Rev 1| User Supplemental Information,
Proteus® Patch
Page 1 of 1
Effective: 19DEC2013
1. TECHNICAL INFORMATION
1.1 – Classification
Caution: Federal (U.S.A) law restricts this device to sale by or on the order of a physician.
The Proteus Patch is categorized as Class II (in US) and IIa (in EU).
The User (patient) is the intended Operator of the Proteus Patch.
1.2 – Environmental Conditions
The Proteus® Patch is intended for storage and operation in a room‐temperature environment.
Condition
Temperature
Humidity
Pressure (Altitude)
Operating
15% ‐ 93%
700 hPa – 1060 hPa
20C – 28C
Storage
20C – 28C
15% ‐ 93%
700 hPa – 1060 hPa
Transport
2C – 38C
15% ‐ 85%
700 hPa – 1060 hPa
1.3 – Minimizing Skin Irritation
The Proteus Patch has been designed to minimize the possibility of skin irritation. Observing these
cautions will reduce the likelihood of skin irritation or bruising under the Patch:
DO NOT continue use until further instruction by a physician if your skin is irritated or
inflamed around the patch.
DO NOT place in locations where your skin is scraped, cracked, inflamed, or irritated.
DO NOT place in a location that overlaps the area of the most recently removed Patch.
DO NOT use if you are allergic to adhesive tape.
DO NOT wear the same Patch for more than one week.
DO NOT drop or bump with excessive force.
1.4 – Protection against Ingress of Solids and Liquids
The Proteus Patch has an Ingress Protection rating of IP27. This means that the enclosure has no
penetrations and it has been rated for immersion in liquid up to 1m depth. For continued safety,
should the enclosure become penetrated or torn, remove the Patch immediately and replace it with
a new one.
1.5 – Avoiding Unsafe Use Conditions
The Proteus Patch is not a diagnostic device. DO NOT attempt to use it to diagnose heart‐related
conditions, an incorrect diagnosis may result.
LBL‐0176, Rev 1| User Supplemental Information,
Proteus® Patch
Page 2 of 2
Effective: 19DEC2013
The Proteus Patch has not been tested or approved as safe for operation during air travel. DO NOT
use the Patch during air travel; it may interfere with the aircraft navigational instruments.
The Proteus Patch has not been tested or approved for use in the presence of strong magnetic or
electric fields. DO NOT wear the Patch during magnetic resonance imaging (MRI), cautery, and
external defibrillation procedures. Damage to the Patch, your skin, or an unexpected magnetic
attraction may result. Please inform your healthcare professional that the Patch must be removed
prior to engaging in one of these procedures.
WARNING: No modification of this equipment is allowed. Modifying the Proteus Patch may cause a
safety hazard for the user.
1.6 – Information on Electromagnetic and Other Interferences
The Proteus Patch has been evaluated and deemed compliant with the requirements in EN60601‐1‐
2 Class B for Electromagnetic Compatibility (EMC). Medical Electrical Equipment needs special
precautions regarding EMC and needs to be installed and put into service according to the EMC
information provided in this User Manual. Portable and mobile RF communications equipment can
affect Medical Electrical Equipment. The Proteus Patch should not be used adjacent to or stacked
with other electromagnetic equipment. If adjacent or stacked use with other electromagnetic
equipment is necessary, verify that the Proteus Patch operation is normal in the configuration(s) in
which it will be used.
1.7 – Information on the Radio Subsystem
The Proteus Patch incorporates a BluetoothTm radio subsystem which is compliant with the
Bluetooth standard. The following information is provided to satisfy the requirements of EN/IEC
60601‐1‐2:
The Bluetooth radio transmits and receives on 40 frequency bands which are equally spaced at
2MHz intervals between 2402MHz and 2480MHz.
The effective receive bandwidth is 1.25MHz.
The transmit modulation is frequency‐hopping using GFSK (Gaussian Frequency Shift Keying) with a
bandwidth‐bit period product BT=0.5. The Modulation index is between 0.28 and 0.35.
The effective radiated power is ‐15dBm ( P = 0.032mW )
Guidance and manufacturer’s declaration – electromagnetic emissions
The Proteus Patch is intended for use in the electromagnetic environment specified below. The
customer or the user of Proteus Patch should assure that it is used in such an environment.
Emissions test
Compliance
Electromagnetic environment – guidance
RF emissions
Group 1
The Patch uses RF energy only for its internal function.
CISPR 11
Therefore, its RF emissions are very low and are not likely
LBL‐0176, Rev 1| User Supplemental Information,
Proteus® Patch
Page 3 of 3
Effective: 19DEC2013
RF emissions
CISPR 11
Harmonic
emissions
IEC 61000‐3‐2
Voltage
fluctuations/
flicker emissions
IEC 61000‐3‐3
Class B
Not applicable
to cause any interference in nearby electronic equipment.
The Patch is suitable for use in all establishments,
including domestic establishments and those directly
connected to the public low voltage power supply
network that supplies buildings used for domestic
purposes.
Not applicable
LBL‐0176, Rev 1| User Supplemental Information,
Proteus® Patch
Page 4 of 4
Effective: 19DEC2013
Guidance and manufacturer’s declaration – electromagnetic immunity
The Proteus Patch is intended for use in the electromagnetic environment specified below. The
customer or the user of the Patch should assure that it is used in such an environment.
Immunity test
IEC 60601 test level
Compliance
Electromagnetic environment –
level
guidance
Electrostatic
+/‐ 6kV contact
+/‐ 6kV
Floors should be wood, concrete
discharge (ESD) IEC +/‐ 8kV air
contact
or ceramic tile. If floors are
61000‐4‐2
+/‐ 8kV air
covered with synthetic material,
the relative humidity should be at
least 30%.
Electrical fast
+/‐ 2 kV for power
Not applicable
transient / burst
supply lines
IEC 61000‐4‐4
+/‐ 1 kV for
input/output
lines
Surge IEC 61000‐4‐ +/‐ 1 kV line(s) to
Not applicable
line(s)
+/‐ 2 kV line(s) to earth
Voltage dips, short <5 % UT (>95 % dip in
Not applicable
UT)
interruptions and
voltage variations
for 0,5 cycle
on power supply
40 % UT (60 % dip in UT)
input lines
for 5 cycles
70 % UT (30 % dip in UT)
IEC 61000‐4‐11
for 25 cycles
<5 % UT (>95 % dip in
UT)
for 5 s
Power frequency
3A/m
3A/m
Power frequency magnetic fields
(50/60 Hz)
should be at levels characteristic
magnetic field
of a typical location in a typical
IEC 61000‐4‐8
commercial or hospital
environment.
NOTE UT is the a.c. mains voltage prior to application of the test level.
Guidance and manufacturer’s declaration – electromagnetic immunity
The Proteus Patch is intended for use in the electromagnetic environment specified below. The
customer or the user of the Proteus Patch should assure that it is used in such an environment.
Immunity test
IEC 60601
Compliance
Electromagnetic environment –
test level
level
guidance
Portable and mobile RF
communications equipment should be
LBL‐0176, Rev 1| User Supplemental Information,
Proteus® Patch
Page 5 of 5
Effective: 19DEC2013
used no closer to any part of the
Proteus Patch, including cables, than
the recommended separation
distance calculated from the equation
applicable to the frequency of the
transmitter.
Recommended separation distance
Conducted RF
IEC 61000‐4‐6
Radiated RF
IEC 61000‐4‐3
3 Vrms
150 kHz to 80
MHz
Not
Applicable
3 V/m
80 MHz to 2,5 GHz
3 V/m
Not Applicable
d = 1,17 √P 80 MHz to 800 MHz
d = 2,33 √P 800 MHz to 2,5 GHz
where P is the maximum output
power rating of the transmitter in
watts (W) according to the transmitter
manufacturer and d is the
recommended separation distance in
metres (m).
Field strengths from fixed RF
transmitters, as determined by an
electromagnetic site survey,a should
be less than the compliance level in
each frequency range.b
Interference may occur in the vicinity
of equipment marked with the
following symbol:
NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.
Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless)
telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast
cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to
fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field
strength in the location in which the Proteus Patch is used exceeds the applicable RF compliance
level above, the Proteus Patch should be observed to verify normal operation. If abnormal
performance is observed, additional measures may be necessary, such as re‐orienting or relocating
the Proteus Patch.
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
LBL‐0176, Rev 1| User Supplemental Information,
Proteus® Patch
Page 6 of 6
Effective: 19DEC2013
Recommended separation distances between portable and mobile
RF communications equipment and the Proteus Patch
The Proteus Patch is intended for use in an electromagnetic environment in which radiated RF
disturbances are controlled. The customer or the user of the Patch can help prevent
electromagnetic interference by maintaining a minimum distance between portable and mobile RF
communications equipment (transmitters) and the Proteus Patch as recommended below,
according to the maximum output power of the communications equipment.
Rated maximum
Separation distance according to frequency of transmitter
output power of
150 kHz to 80 MHz
80 MHz to 800 MHz
800 MHz to 2.5 GHz
transmitter
d = 1,2 √P
d = 1,2 √P
d = 2,3 √P
0.01
Not applicable
0.1
0.23
0.1
Not applicable
0.4
0.74
Not applicable
1.2
2.3
10
Not applicable
3.7
7.4
100
Not applicable
12
23
For transmitters rated at a maximum output power not listed above, the recommended separation
distance d in meters (m) can be estimated using the equation applicable to the frequency of the
transmitter, where P is the maximum output power rating of the transmitter in watts (W) according
to the transmitter manufacturer.
NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.
1.8 – European R&TTE Declaration of Conformity
Hereby, Proteus® Digital Health, Inc., declares that the Proteus Patch is in compliance with the
essential requirements and other relevant provisions of R&TTE (Radio and Telecommunications
Terminal Equipment) Directive 1999/5/EC. The product is compliant with the following standards
and/or other normative documents:
Safety (art. 3.1a):
EN 60601‐1, 3rd Ed, IEC 60601‐1‐11
EMC (art. 3.1b):
EN 301 489‐17 v2.2.1
Spectrum (art. 3.2):
EN 300 328 v1.8.1
Other:
EN 60601‐1‐2 (2007)
The Proteus Patch can be used in countries in the European Union.
1.9 – CISPR Interference Statement
MEDICAL ELECTRICAL EQUIPMENT needs special precautions regarding EMC and needs to be
installed and put into service according to the EMC information provided in this section of the
manual. Portable and mobile RF communications equipment can affect MEDICAL ELECTRICAL
LBL‐0176, Rev 1| User Supplemental Information,
Proteus® Patch
Page 7 of 7
Effective: 19DEC2013
EQUIPMENT. The Proteus Patch may be interfered with by other equipment, even if that equipment
complies with CISPR emission requirements.
1.10 – FCC Interference Statement
This device complies with Part 15 of the FCC Rules. Operation is subject to the following two
conditions: (1) this device may not cause harmful interference, and (2) this device must accept any
interference received, including interference that may cause undesired operation. Changes or
modifications not expressly approved by Proteus Digital Health could void your authority to operate
the equipment.
1.11 – FCC Wireless Notice
This product emits radio frequency energy, but the radiated output power of this device is far below
the FCC radio frequency exposure limits.
Note:
This equipment has been tested and found to comply with the limits for a Class B digital device,
pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable protection
against harmful interference in a residential installation. This equipment generates, uses and can
radiate radio frequency energy and, if not installed and used in accordance with the instructions,
may cause harmful interference to radio communications. However, there is no guarantee that
interference will not occur in a particular installation. If this equipment does cause harmful
interference to radio or television reception, which can be determined by turning the equipment off
and on, the user is encouraged to try to correct the interference by one or more of the following
measures:
— Reorient or relocate the receiving antenna.
— Increase the separation between the equipment and receiver.
— Connect the equipment into an outlet on a circuit different from that to which the receiver is
connected.
— Consult the dealer or an experienced radio/TV technician for help.
1.12 – FCC Identifier
FCC ID: X7906120
2 – DISPOSAL OF WASTE PRODUCTS
Production of this equipment required the extraction and use of natural resources. The equipment
may contain substances that could be harmful to the environment or human health if improperly
handled at the product’s end of life. In order to avoid release of such substances into the
environment and to reduce the use of natural resources, all devices, both used and unused, should
not be disposed with household waste. Return to a recycling point for electric and electronic
devices.
LBL‐0176, Rev 1| User Supplemental Information,
Proteus® Patch
Page 8 of 8
Effective: 19DEC2013
3 – MANUFACTURER CONTACT INFORMATION
To request technical information or to report unexpected events, please contact the manufacturer
at one of these locations.
United States
United Kingdom
Proteus Digital Health UK Ltd
6th Floor, 41‐44 Great Queen St.
London WC2B 5AD
Proteus Digital Health, Inc
2600 Bridge Parkway, Suite 101
Redwood City, CA 94065
Phone Number: 650‐632‐4031
Fax Number: 650‐632‐4071
LBL‐0176, Rev 1| User Supplemental Information,
Proteus® Patch
Page 9 of 9
Effective: 19DEC2013

---

Source Exif Data:

File Type                       : PDF
File Type Extension             : pdf
MIME Type                       : application/pdf
PDF Version                     : 1.5
Linearized                      : Yes
Author                          : jhutchison
Create Date                     : 2014:01:14 15:59:54-08:00
Modify Date                     : 2014:01:14 15:59:54-08:00
XMP Toolkit                     : Adobe XMP Core 5.2-c001 63.139439, 2010/09/27-13:37:26
Format                          : application/pdf
Creator                         : jhutchison
Title                           : Microsoft Word - LBL-0176 Rev 1 DW5 Patch User Supplemental Information.docx
Creator Tool                    : PScript5.dll Version 5.2.2
Producer                        : Acrobat Distiller 10.1.8 (Windows)
Document ID                     : uuid:19ea9bfd-fbc9-4f44-9140-081c57e842c0
Instance ID                     : uuid:02982229-e4a9-4e9c-b712-6ac2f7ba0f19
Page Count                      : 9

EXIF Metadata provided by EXIF.tools