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Developed by a physician, Buzzy® is a
reusable devic
e for minor aches and pains.
Buzzy
®
Healthcare is for use in a professional healthcare facility
by trained operator. Reusable pain relief product intended for
multiple users. Thoroughly clean and disinfect Buzzy
®
and its
accessories between
patients following
your facility’s
infection
control protocol for reprocessing non-critical equipment.
BuzzyHelps.c
om
For Buzzy
®
Mini Healthcare (Striped, Black, and LadyBuzz)
and Buzzy
®
XL Healthcare (Striped, Black, and LadyBuzz)
BKHM1, BKHM2, BKHM3, BTH1, BTH2, BTH3
IFU-001 Rev 00 Buzzy Healthcare Instructions for Use
09.17.2020
Indications For Use:
Controls pain associated with injections (venipuncture, IV
starts, cosmetic procedures) and the temporary relief of
minor injuries (muscle or tendon aches, splinters and bee
stings). Also intended to treat myofascial pain caused by
trigger points, restricted motion and muscle tension.
Warnings:
For intended use only • Direct or prolonged application of ice
could vasoconstrict or alter lab values.
Contraindications:
Do not use in the presence of unexplained calf pain. Consult
a physician. • This device should not be used over swollen or
inflamed areas or skin eruptions. • Do not place directly on a
thermal burn • Do not use ice pack with underlying sensitivities
to ice or cold (e.g. Sickle Cell Disease, Reynaud’s Disease).
Cautions:
Store wings in a cool, dry place. • Wings must be frozen solid
for best effect. • Do not use dry ice to freeze wings unless
supervised by a healthcare professional • Do not puncture ice
pack chambers. • Discard if leaking. • Do not ingest gel. • Keep
out of reach of children or pets. • Do not use with neuropathy,
CRPS, or sensitivities to ice.
Model Differences:
Buzzy
®
Mini: Comes with Buzzy
®
vibration unit with button
switch and energy saving automatic 3-minute shut-off, four
reusable ice wings and 1 Comfort Strap, and instructions. Press
and hold button firmly until vibration activates.
Buzzy
®
XL: Comes with Buzzy
®
vibration unit with toggle switch,
four reusable ice wings and 2 Comfort Straps, and instructions.
Keep the tape on the switch during transport to avoid accidental
activation. Activate with the on/off toggle switch.
Cleaning:
Buzzy
®
is
a reusable medical
device that
should be
thoroughly
cleaned and
reprocessed following
your facility’s
infection
control protocol for non-critical equipment. All accessories
must be cleaned
and disinfected
with your
facility’s disinfecting
wipes or method used to reprocess non-critical equipment
such as stethoscopes or patient monitors. Do not autoclave.
Do not immerse in liquid.
Batt
eries:
Unscrew the back using a Phillips-head screwdriver to remove
back panel. Buzzy
®
is powered by 2 alkaline AAA batteries. Remove
batteries if Buzzy
®
is not being used for extended period of time.
Disposal:
Please contact
your local
authorities to
determine the
proper
method of
disposal of
potentially biohazardous
parts and
accessories.
DO NOT SERVICE WHILE IN USE
US Patented British Patent No. 2455695
RM-1910, 1248-064-5002-00, 1248-064-5001-00
Troubleshooting:
With proper
care, your
Buzzy should
last for at
least 1
year. With
heavy use
or extreme
temperature fluctuations,
batteries may need to be replaced more frequently. If device
stops working,
replace batteries.
Press switch
firmly
for 1/2
second to activate or turn off.
How To Or
der/Additional Inf
ormation:
Please visit
our website
buzzyhelps.com for
a complete
list of FAQ’s,
other pain management tips, how-to
videos,
accessories, replacement parts, and more!
Guaran
tee:
Previous medical
history and
intrinsic physiologic
differences
may make Buzzy
®
less
effective for
some people.
If
not
completely satisfied,
return within
30 days
to place
of
purchase for a full refund,
or contact us at the address below.
MMJ Labs, LLC dba Pain Care Labs
322 Sutherland Place • Atlanta, GA 30307, U.S.A.
buzzyhelps.com • [email protected]
877.805.2899
Authorized European Representative
MPC International S.A.
26, Boulevard Royal • L-2449 Luxembourg
Tel. +352 22 99 99 5546 | www.mpc.cc
M
ad
e fr
om
at le
ast 30% post con
sum
er
w
as
te
10
0%
Bio
degradable Packa
gin
g
Indications For Use .......................................... 1
Warnings, Contraindications, Cautions ......... 1
Model Differences ............................................ 2
Directions For Use ........................................... 3
Ice Wings ................................................... 3, 4
For Injections ................................................ 5
Buzzy
®
Placement ............................................ 5
Finger Sticks, Splinters ................................ 7
Stomach Injections ...................................... 7
Burning, Itching ............................................ 7
IVs & Phlebotomy, For children .................. 8
Cleaning, Changing Batteries, Disposal ......... 9
Troubleshooting, Ordering, Guarantee ....... 10
Environmental conditions:
Transport and storage
between uses: -25 to 70 °C.
0-95% RH. 700-1060 hPa
Operating conditions:
5-40 °C. 15-95% RH
700-1060 hPa. 2000m altitude
ON
OFF
1. 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.
2. “Please note that changes or modifications of this product is not expressly approved by the party
responsible for compliance could void the user’s authority to operate the equipment.”
3. 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.
4. 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. Pain Care Labs, 195 Arizona Ave • LW08 NE Atlanta GA 30307 • 877-805-2899
(Pain Care Labs Responsible Party in USA.)
Type BF Applied Part
DRAFT
