Uds B
Uds B
Uds B
1
or with oxygen or nitrous oxide.
1.4 Installation of the main components
1.4.1 Sketch map for installation and connection
a) The top and side map of the equipment
picture 1(a)
picture 1(b)
b) Sketch map for connection of foot switch, power supply and main unit.
2
picture 2
piture 3
3
picture 4
e) Sketch map for installing tip with wrench.
picture 5
4
2.2.7 Select a suitable scaling tip as you need, screw it on the handpiece
tightly by the wrench (picture 5).
2.2.8 The normal frequency is extremely high. Under the normal working
state of the scaling tip, a light touch and a certain to-and-fro motion will
eliminate the tartar without heating. Overexertion and long-time lingering are
forbidden.
2.2.9 Vibrating intensity: adjust the vibration intensity as you need, generally
turn the knob to the middle grade. According to patients' different sensitivity
and the rigidity of the gingival tartar, adjust the vibration intensity during the
clinical treatment.
2.2.10 Water volume adjustment: step on the foot switch, and the tip begins
to vibrate, then turn the water control knob to form fine spray to cool down the
handpiece and rinse the teeth.
2.2.11 The handpiece can be handled in the same gesture as a pen in hand.
2.2.12 During the clinical treatment, be sure not to make the end of tip touch
the teeth vertically and not to make the tip overexert on the surface of the teeth in
case of hurting the teeth and damaging the tip.
2.2.13 Afier finishing operation, keep the machine working for 30 seconds on
the water supply condition in order to rinse the handpiece and the scaling tip.
Notice: Don't screw off the scaling tips when the foot switch is stepped on
and the machine is working.
5
3. Maintenance
3.1 Troubleshooting
If the problem still can’t be solved, please contact with local dealer or
manufacturer.
3.2 Notice
[Note l] Turn the water control knob toward direction of symbol till not be able
to turn any more, it comes to the min; on the contrary direction, the water volume
6
increases step by step till not be able to turn anymore.
[Note 2] Clean the water pipe with the multi-function syringe of the dental
unit (as showed in picture 6):
① Cut the water pipe at a distance of 10cm~20cm from the water entrance.
② Turn on the electricity and get through to the power.
③ Connect the multi-function syringe of dental unit to the water pipe.
④ Disassemble the tip or handpiece.
⑤ Step on the foot switch.
⑥ Turn on the switch of the multi-function syringe, press the water into the
machine and the impurity blocked in the water pipe can be eliminated.
[Note 3] If the scaling tip has been screwed on tightly and there is fine spray,
the following phenoruena shows that the scaling tip is damaged:
① The vibrating intensity and the water atomization degree become weak
obviously.
② During treatment, it produces the sound like "buzz" from the scaling tip.
7
4.1 Initial processing
4.1.1 Processing principles
It is only possible to carry out effective sterilization after the completion of
effective cleaning and disinfection. Please ensure that, as part of your responsibility
for the sterility of products during use, only sufficiently validated equipment and
product-specific procedures are used for cleaning/disinfection and sterilization, and
that the validated parameters are adhered to during every cycle.
Please also observe the applicable legal requirements in your country as well
as the hygiene regulations of the hospital or clinic,especially with regard to the
additional requirements for the inactivation of prions.
4.1.2 Post-operative treatment
The post-operative treatment must be carried out immediately, no later than 30
minutes after the completion of the operation. The steps are as follows:
Tools: Endo wrench or 1# torque wrench, tray, clean and dry soft cloth
1. Let the UltrasonicScaler works for 20-30 seconds at maximum water volume
to flush the handpiece and tip;
2. Soak the soft cloth with pure water (or distilled water or deionized water),
and then wipe all the surfaces of the handpiece and tip until the surface of them is
not stained;
3. Dry the handpiece and tip with a clean, soft cloth;
4. Remove the tip from handpiece with Endo wrench or 1# torque wrench
provided by Guilin Woodpecker Medical Instrument Co., Ltd, and then put the tip
and wrench into a clean tray.
Notes
a) The water used here must be pure water, distilled water or deionized water.
4.2Cleaning
The cleaning should be performed no later than 24 hours after the operation.
The cleaning can be divided into automated cleaning and manual cleaning.
Automated cleaning is preferred if conditions permit.
4.2.1Automated cleaning
•The cleaner is proved to be valid by CE certificationin accordance with EN
ISO 15883.
▪There should be a flushing connector connected to the inner cavity of the
product.
▪The cleaning procedure is suitable for the product, and the irrigating period is
sufficient.
It is recommended to use a washer-disinfector in accordance with EN ISO
15883. For the specific procedure, please refer to the automated disinfection section
in the next section "Disinfection".
Notes
a) The cleaning agent does not have to be pure water.It can be distilled water,
deionized water or multi-enzyme. But please ensure that the selected cleaning
8
agent is compatible with the product.
b) In washing stage, the water temperature should not exceed 45 °C, otherwise
the protein will solidify and it would be difficult to remove.
c) After cleaning, the chemical residue should be less than 10mg / L.
4.3Disinfection
Disinfection must be performed no later than 2 hours after the cleaning phase.
Automated disinfection is preferred if conditions permit.
4.3.1 Automated disinfection-Washer-disinfector
•The washer-disinfector is proved to be valid by CE certification in accordance
with EN ISO 15883.
•Use high temperature disinfection function. The temperature does not exceed
134 ° C, and the disinfection under the temperature cannot exceed 20 minutes.
•The disinfection cycle is in accordance with the disinfection cycle in EN ISO
15883.
Cleaning and disinfecting steps by using Washer-disinfector
1. Carefully place the product into the disinfection basket. Fixation of product
is neededonly when the product is removable in the device. The products are not
allowed to contact each other.
2. Use a suitable rinsing adaptor, and connect the internal water lines to the
rinsing connection of the washer-disinfector.
3. Start the program.
4. After the program is finished, remove theproductfrom the washer-disinfector,
inspect (refer to section "Inspection and Maintenance") and packaging (refer to
chapter "Packaging"). Dry the productrepeatedly if necessary (refer to section
"Drying").
Notes
a)Before use, you must carefully read the operating instructions provided by the
equipment manufacturer to familiarize yourself with the disinfection process and
precautions.
b)With this equipment, cleaning, disinfection and drying will be carried out
together.
c)Cleaning: (c1)The cleaning procedure should be suitable for the product to
be treated. The flushing period should be sufficient (5-10 minutes). Pre-wash for 3
minutes, wash for another 5 minutes, and rinse it for twice with each rinse lasting
for 1 minute. (c2) In the washing stage, the water temperature should not exceed
45 °C, otherwise the protein will solidify and it is difficult to remove. (c3) The
solution used can be pure water, distilled water, deionized water or multi-enzyme
solution, etc., and only freshly prepared solutions can be used.(c4)During the use
of cleaner, the concentration and time provided by manufacturer shall be obeyed.
The used cleaner is neodisherMediZym (Dr. Weigert).
d)Disinfection: (d1) Direct use after disinfection: temperature ≥ 90 ° C, time ≥ 5
min or A0 ≥ 3000;
(d2)Sterilize it after disinfection and use: temperature ≥ 90 ° C, time ≥ 1 min or
9
A0 ≥ 600
(d3) For the disinfection here,the temperature is 93 ° C, the time is 2.5 min,
and A0>3000
e) Only distilled or deionized water with a small amount of microorganisms
(<10 cfu/ml) can be used for all rinsing steps. (For example, pure water that
is in accordance with the European Pharmacopoeia or the United States
Pharmacopoeia).
f) After cleaning, the chemical residue should be less than 10mg / L.
g)The air used for drying must be filtered by HEPA.
h) Regularly repair and inspect the disinfector.
4.4Drying
If your cleaning and disinfection process does not have an automatic drying
function, dry it after cleaning and disinfection.
Methods
1. Spread a clean white paper (white cloth) on the flat table, point the product
against the white paper (white cloth), and then dry the product with filtered dry
compressed air (maximum pressure 3 bar). Until no liquid is sprayed onto the
white paper (white cloth), the productdrying is completed.
2. It can also be dried directly in a medical drying cabinet (or oven). The
recommended drying temperature is 80℃~120℃ and the time should be 15~40
minutes.
Notes
a) The drying of product must be performed in a clean place.
b) The drying temperature should not exceed 138 °C;
c) The equipment used should be inspected and maintained regularly.
4.5Inspection and maintenance
In this chapter, we only check the appearance of the product.
4.5.1 Check theproduct. If there is still visible stain on the product after
cleaning/disinfection, the entire cleaning/disinfection process must be repeated.
4.5.2 Check theproduct. If it is obviously damaged, smashed, detached,
corroded or bent, it must be scrapped and not allowed to continue to be used.
4.5.3 Check theproduct. If the accessories are found to be damaged, please
replace it before use. And the new accessories for replacement must be cleaned,
disinfected and dried.
4.5.4 If the service time (number of times) of the product reaches the specified
service life (number of times), please replace it in time.
4.6Packaging
Install the disinfected and driedproductand quickly package it in a medical
sterilization bag (or special holder, sterile box).
Notes
a) The package used conforms to ISO 11607;
10
b) It can withstand high temperature of 138 °C and has sufficient steam
permeability;
c) The packaging environment and related tools must be cleaned regularly to
ensure cleanliness and prevent the introduction of contaminants;
d) Avoid contact with parts of different metals when packaging.
4.7Sterilization
Use only the following steam sterilization procedures (fractional pre-vacuum
procedure*) for sterilization, and other sterilization procedures are prohibited:
1. The steam sterilizer complies with EN13060 or is certified according to EN
285 to comply with EN ISO 17665;
2. The highest sterilization temperature is 138 ° C;
3. The sterilization time is at least 4 minutes at a temperature of 132 ° C / 134
° C and a pressure of 2.0 bar ~ 2.3 bars.
4. Allow a maximum sterilization time of 20 minutes at 134 °C.
Verification of the fundamental suitability of the products for effective steam
sterilization was provided by a verified testing laboratory.
Notes
a) Only products that have been effectively cleaned and disinfected are
allowed to be sterilized;
b) Before using the sterilizer for sterilization, read the Instruction Manual
provided by the equipment manufacturer and follow the instructions;
c) Do not use hot air sterilization and radiation sterilization as this may result
in damage to the product;
d) Please use the recommended sterilization procedures for sterilization. It is
not recommended to sterilize with other sterilization procedures such as ethylene
oxide, formaldehyde and low temperature plasma sterilization. The manufacturer
assumes no responsibility for the procedures that have not been recommended.
If you use the sterilization procedures that have not been recommended, please
adhere to related effective standards and verify the suitability and effectiveness.
*Fractional pre-vacuum procedure = steam sterilization with repetitive pre-
vacuum.The procedure used here is to perform steam sterilization through three
pre-vacuums.
4.8Storage
4.8.1Store in a clean, dry, ventilated, non-corrosive atmosphere with a relative
humidity of 10% to 93%, an atmospheric pressure of 70KPa to 106KPa, and a
temperature of -20 °C to +55 °C;
4.8.2After sterilization,the product should be packaged in a medical
sterilization bag or a clean sealing container, and stored in a special storage
cabinet. The storage time should not exceed 7 days. If it is exceeded, it should be
reprocessed before use.
Notes
11
a)The storage environment should be clean and must be disinfected regularly;
b) Product storage must be batched and marked and recorded.
4.9Transportation
1.Prevent excessive shock and vibration during transportation, and handle with
care;
2. It should not be mixed with dangerous goodsduring transportation.
3. Avoid exposure to sun or rain or snow during transportation.
The cleaning and disinfection of main unit and handpiece are as follows.
1 Pre-Op processing
Before each use, the handpiece and main unitmust be cleaned and disinfected.
The specific steps are as follows:
1.1 Manual cleaning steps:
1.1.1 Wet the soft cloth completely with distilled water or deionized water, and
then wipe all the surfaces of the handpiece and main unit until the surface of them
is not stained.
1.1.2 Wipe the surface of the handpiece and main unit with a dry soft nap-free
cloth.
1.1.3 Repeat the above steps at least 3 times.
Notes:
a) Use distilled water or deionized water for cleaning at room temperature.
1.2 Manual disinfection steps:
1.2.1 Soak the dry soft cloth with 75% alcohol
1.1.2 Wipe all the surfaces of the handpiece and main unitwith a wet soft cloth
for at least 3 minutes.
1.1.3 Wipe the surface of the handpiece and main unit with a dry soft nap-free
cloth.
Notes:
a) The cleaning and disinfection must be performed within 10min before use.
b) The disinfectant used must be used immediately, no foaming is allowed.
c) In addition to 75% alcohol, you can use non-residue disinfectants such as
Oxytechfrom Germany, but you must respect the concentration, temperature and
time specified by the disinfectant manufacturer.
2 Post-Op processing
After each use, clean and disinfect the handpiece and main unit within 30
minutes. The specific steps are as follows:
Tools: Nap-free soft cloth, tray
2.1 Remove the tip from handpiece with Endo wrench or 1# torque wrench
provided by Guilin Woodpecker Medical Instrument Co., Ltd, and then put the tip
and wrench into a clean tray.
2.2 Soak the nap-free soft cloth with distilled water or deionized water, and
then wipe all the surfaces of the handpiece andmain unituntil the surface of them
is not stained.
12
2.3 Wet the dry soft cloth with 75% alcohol, and then wipe all surfaces of the
handpiece andmain unit for 3 minutes.
2.4 Put the handpiece and main unit back into the clean storage area.
Notes:
a) The cleaning and disinfection must be performed within 10min before use.
b) The disinfectant used must be used immediately, no foaming is allowed.
c) In addition to 75% alcohol, you can use non-residue disinfectants such as
Oxytechfrom Germany, but you must respect the concentration, temperature and
time specified by the disinfectant manufacturer.
5. Precaution
5.1 Notice when using equipment
5.1.1 Keep the scaler clean before and after operation.
5.1.2 The handpiece, scaling tip and wrench must be sterilized before every
treatment.
5.1.3 Don't screw or unscrew the scaling tip when stepping on the foot switch.
5.1.4 The scaling tip must be fastened and there must be fine spray coming
out from the tip when operating.
5.1.5 Change a new one when the tip is damaged or worn excessively.
5.1.6 While scaler working ,the heat of scaling tip will become higher if there
is no water flowing out.Please keep the water flow smoothly.
5.1.7 Don't twist or rub the tip.
5.1.8 Don't use impure water source and be sure not use normal brine instead
of pure water source.
5.1.9 If use the water source without hydraulic pressure, the water surface
should be one meter higher than the head of the patient.
5.1.10 Don't pull the cable forcibly in case of the handpiece falling off from
the cable.
5.1.11 Don't knock or rub the handpiece.The modified content of instruction:
5.1.12 Please put the power plug into the socket easy to pull out, to make sure
it can be pull out in emergency.
5.1.13 The power supply is considered as a part of ME equipment.This device
can only be equipped with the special power supply of Guilin Woodpecker
Medical Instrument Co., Ltd.
5.1.14 The power supply is not waterproof. Please keep it dry and away from
the water.
5.1.15 After operating, turn off the power, then pull out the plug.
5.1.16 We are only responsible for the safety on the following conditions:
a) The maintenance, repair and modification are made by the manufacturer or
the authorized dealer.
b) The changed components are original of "WOODPECKER" and operated
according to instruction manual.
13
5.1.17 The internal screw thread of the scaling tips produced by some other
manufactures maybe coarse, rusty and collapsed. This will damage the external
screw thread of the handpiece irretrievably. Please use "WOODPECKER" brand
scaling tips.
5.1.18 Please select a suitable power when using different type of tips (refer to
"TABLE OF OPERATING POWER OF THE TIPS").
5.2 Contraindication
5.2.1 The hemophilia disease patient is not allowed to use this equipment.
5.2.2 The patients or doctors with heart pacemaker are forbidden to use this
equipment.
5.2.3 The heart disease patient, pregnant woman and children should be
cautious to use the equipment.
5.3 Storage and maintenance
5.3.1 The equipment should be handled carefully and lightly. Be sure that it is
far from the vibration, and installed or kept in a cool, dry and ventilated place.
5.3.2 Don't store the machine together with the articles that are combustible,
poisonous, caustic, and explosive.
5.3.3 This equipment should be stored in a room where the relative humidity
is 10% ~ 93%, atmospheric pressure is 70kPa to106kPa, and the temperature is
-20°C ~ +55°C.
5.3.4 If not be used for a long time, please make the machine get through to
the electricity and water once per month for five minutes.
5.4 Transportation
5.4.1 Excessive impact and shake should be prevented in transportation. Lay it
carefully and lightly and keep it upright.
5.4.2 Don't put it together with dangerous goods during transportation.
5.4.3 Avoid solarization and getting wet in rain or snow during transportation.
5.5 Working condition
5.5.1 Environment temperature: +5°C to +40°C
5.5.2 Relative humidity: 30% ~75%
5.5.3 Atmosphere pressure: 70kPa to 106kPa
5.5.4 A temperature of the water at the inlet:not higher than +25°C
6. After-service
We offer one year free repair to the equipment according to the warranty
card. The repair of the equipment should be carried out by our professional
technician. We are not responsible for any irretrievable damage caused by the not
professional person.
14
7. Symbol instruction
8. Environmental protection
Please dispose according to the local laws.
9. Statement
All rights of modifying the product are reserved to the manufacturer without
further notice. The pictures are only for reference. The final interpretation rights
belong to GUILIN WOODPECKER MEDICAL INSTRUMENT CO., LTD.
The industrial design, inner structure, etc, have claimed for several patents by
WOODPECKER, any copy or fake product must take legal responsibilities.
15
TABLE OF OPERATING POWER OF THE TIPS
Scaling Endodontics
Tip Model Power Tip Model Power
G1 1-9 E1 -
G2 1-9 E2 -
G3 1-9 E3 -
G4 1-9 E3D -
G5 1-9 E4 -
G6 1-9 E4D -
G7 1-9 E5 -
G8 1-9 E5D -
G9 1-9 E8 -
G 10 1-9 E9 -
G 11 1-9 E10 -
E10D -
Periodontics E11 -
Tip Model Power E11D -
P1 1-6 E14 -
P2L 1-2 E15 -
P2LD 1
P2R 1-2 Cavity Preparation
P2RD 1 Tip Model Power
P3 1-3 SB1 1-6
P3D 1-3 SB2 1-6
P4 1-3 SB3 1-6
P4D 1-3 SBL 1-6
SBR 1-6
16
ZMN-SM-111 V3.3- 20200509