Rolence Enterprise Inc.
| Payment Type: | T/T,Credit Card |
| Incoterm: | FOB,EXW,CFR,CIF,FCA,FAS,CPT,CIP |
| Transportation: | Ocean,Air,Express |
| Port: | Port of Keelung |
Model No.: MS-50
Brand: ELiTEDENT
Place Of Origin: Taiwan, China
Kind Of Power: Electricity
Warranty Service: 1 Year
After-sales Service: Online Technical Support, Onsite Training, Return And Replacement
Material: Metal, Plastic
Shelf Life: 1years
Product Quality Certification: Ce
Medical Device Classification: Class Ii
Safety Standard: None
| Selling Units | : | Piece/Pieces |
| Package Type | : | By paper box |
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‧Persons who are fitted with cardiac pacemakers, defibrillators and other active implanted medical devices, have been cautioned that some types of electronic equipment might interfere with the operation of the device. We recommend that the MS Handpiece Cable Set be kept at least 6 to 9 inches (15 to 23 cm) away from any device and their leads during use.
‧During using the Ultrasonic Scaler, make sure that water is flowing continuously. If the handpiece overheats please check the water supply, and stop using the Ultrasonic Scaler for a while.
ROLENCE ENTERPRISE INC. is an ISO 9001, ISO 13485 certified manufacturer of Ultrasonic Scalers. All the products are FDA registered and compliant with EN standard (CE Marking).
Conformance to Standards:
The MS-50 R1 Ultrasonic Scaler conforms to IEC60601-1-2:2007 and IEC60601-1-1:2006. The device is CE marked corresponding to European Medical Device Directive (93/42/EEC).
Supplies and Replacement Parts
Contact your local ROLENCE dealer to order supplies or replacement parts. There are no serviceable parts included in the Ultrasonic Scaler. Please contact your dealer to acquire all repairing service and technique supports.
CAUTION: EQUIPMENT NOT SUITABLE FOR USE IN THE PRESENCE OF FLAMMABLE
ANESTHETIC MIXTURE WITH AIR OR WITH NITROUS OXIDE.
CAUTION: U.S FEDERAL LAW RESTRICTS THIS DEVICE TO SALE BY OR ON THE ORDER OF A DENTAL PROFESSIONAL.
Ultrasonic procedure
‧All general supra and subgingival scaling applications.
‧Periodontal debridement for all types of periodontal diseases.
‧Endodontic procedures.
MS-50 R1 Ultrasonic Scaler
Voltage input: 100V, 110V, 230V, 240V
Wattage: MAX. 80 W
Water Pressure: 20 - 40 psi
Dimension:
Height: 19.5 cm
Width: 8.5 cm
Depth: 21.0 cm
Weight: 2500 g
Tip vibration frequency: 25/30 k +/- 3 kHz
Half-excursion force: < 1N
Function:
The MS-50 R1 Ultrasonic Scaler is designed for use in prophylaxis treatments periodontia, and other areas of operative dentistry.
When used in prophylaxis treatment, the unit operates with a fine water spray, requiring little of the physical exertion necessary with hand instruments. It easily and effectively removes stubborn calculus and stains both supragingivally and subgingivally, leaving crown and root surfaces clean and smooth.
General Infection Control
Recommendations
‧As with all dental procedures, the use of standard personal protection equipment (i.e., wearing a face mask, eyewear, or face shield, gloves and protective gown) is recommended.
‧For maximal operator and patient safety, carefully follow section 12 system maintenance and care information detailed in the operating instruction.
‧As with high speed handpieces, and other dental devices, the combination of water and ultrasonic vibration from your MS-50 R1 Ultrasonic Scaler will create aerosols. With proper technique, much of the aerosol dispersion can be effectively controlled and minimized. Please carefully follow the procedural guide lines in this manual regarding the use of your Ultrasonic Scaler.
‧Always flush your MS-50 R1 Ultrasonic Scaler at least 20 seconds with highest flow after each treatment.
‧Clean and disinfect the handpiece sleeve between patients. The handpiece sleeve can be autoclaved up to 135℃ for at least 10 minutes.
Sterilizing:
1. Autoclave: compliant with standard EN 13060.
2. Place sterilizable sleeve of handpiece and pouched ultrasonic insert into a steam autoclave. After warm-up is completed, operate at a sterilizing temperature and pressure of 273° F/31 psi (134°C/216 kPa) for 18 minutes, followed by a
20-30 minute drying time.
3. To maintain sterility, the insert should remain in the sealed pouch until it is ready for use.
DO NOT USE Cold sterilization solution.
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