Jiffy ULT-7024M One Single Use Polishers Instruction Manual

: June 1, 2024
: Jiffy

Table of Contents

Jiffy ULT-7024M One Single Use Polishers
Preparation
CONTACT
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Jiffy ULT-7024M One Single Use Polishers

Jiffy-ULT-7024M-One-Single-Use-Polishers-PRODUCT

Preparation

Preparation and Reprocessing Instructions by DIN/EN ISO 17664

Jiffy-ULT-7024M-One-Single-Use-Polishers-FIG-1

WARNINGS

Observe the manufacturer’s information on material compatibilities for cleaning, disinfection, and sterilization.
All instruments are delivered unsterile and must go through the indicated cycle before and after each use.
Strong acids and strong bases may oxidize the stainless steel shank.
Avoid temperatures >150 ºC
Ultrasonic bath must not exceed temperatures of 42 ºC because of the possible coagulation of protein.
Instruments that have not completely dried after cleaning and disinfection must be dried again (e.g., with medical compressed air) to avoid compromising the success of sterilization.
Instructions of cleaning and/or disinfecting solutions must specifically state “suitable for rubber polishers or synthetics/ silicones.” The exposure time and concentration specified by the manufacturer must be followed.

RESTRICTION OF REPROCESSING
Disposable products delivered unsterile, marked with the symbol ( ), may only go through the validated sterilization cycle ONCE before initial use.

RISK ASSESSMENT AND CLASSIFICATION OF MEDICAL DEVICES BEFORE REPROCESSING

The type and scope of reprocessing is determined by the use of the medical device. Therefore, the operator is responsible for the correct classification of the medical devices and thus for the definition of the type and scope of reprocessing (see KRINKO/BfArM recommendation, point 1.2.1 Risk assessment and classification of medical devices before reprocessing). Based on this user- dependent classification, the operator can determine which of the reprocessing methods listed in this preparation and reprocessing instruction needs to be applied.

PLACE OF USE:	No special requirements.
STORAGE AND TRANSPORT:	It is recommended to transport the contaminated

instruments in a closed container.

It is recommended that instruments be reprocessed as soon as possible, within 2 hours after use at the most. Intermediate storage of used instruments with contamination such as blood residues can lead to corrosion damage.

PREPARATION:| Wear personal protective equipment (durable gloves, water- repellent coat, face protection mask or goggles, and protection mask).

PRE-TREATMENT:

| Pre-clean under running water with a brush (plastic) directly after use.

Equipment: Plastic brush (e.g., Interlock, #09084), tap water (20±2 ºC) (at least drinking water quality)

1. Rinse the polishers under running water for 60 seconds and brush them thoroughly with a plastic brush, particularly the difficult-to-access areas of the head (bristles, silicone bristle tips).

CLEANING: MANUAL

| Note: Coarse surface contamination on the instruments must be removed before manual reprocessing (see pre-treatment). Equipment: Multi-stage enzymatic cleaner (e.g., Dürr Dental, Id 215), tap water/flowing water (20±2ºC) (at least drinking water quality), ultrasonic bath (e.g., Sonorex Digital 10P).

1. Prepare the cleaning solution according to the manufacturer’s instructions (Dürr Dental ID 215 2% solution was validated) and fill it into an ultrasonic bath.

2. Completely immerse the polishers in the solution.

3. Expose the products for 1 minute to the ultrasonic bath.

4. Remove the polishers from the cleaning solution and rinse them thoroughly (30 seconds) under running water.

5. Check for cleanliness. If contamination is still visible, repeat the above-specified steps.

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DISINFECTION: MANUAL

| Equipment: At least limited virucidal instrument disinfectant (VAH listed—or at least listed in the IHO with testing according to DW) e.g., based on quaternary ammonium compound(s), alkylamine(s)/alkylamine derivative(s), guanidine(s)/guanidine derivative(s) (e.g., Dürr Dental, ID 212), preferably fully deionized water (deionized water, according to KRINKO/BfArM

recommendation free of facultatively pathogenic microorganisms), ultrasonic bath (e.g., Sonorex Digital 10P), and lint-free sterile cloth.

1. Prepare the disinfectant solution according to the manufacturer’s instructions (Dürr Dental ID 212, 2% solution was validated) and place it into an ultrasonic bath.

2. Completely immerse the polishers in the disinfectant solution.

3. Expose the products for 2 minutes to the ultrasonic bath.

4. Further exposure time to the disinfectant solution for 5 minutes according to the disinfectant manufacturer’s instructions.

5. Remove the polishers from the disinfectant solution and allow them to drip off.

6. Rinse the products with deionized water for 30 seconds.

7. Wipe with a single-use sterile lint-free cloth or, if necessary, dry with medical compressed air.

CLEANING AND DISINFECTION: AUTOMATIC

| Note: Coarse surface contamination on the instruments must be removed before automatic reprocessing (see pre-treatment). Equipment: Cleaning and disinfection unit according to DIN EN ISO 15883-1+2 with the thermal program (temperature 90 ºC to 95 ºC), detergent: mildly alkaline detergent (e.g., Dr. Weigert neither MediClean Dental).

1. Place the instruments in a suitable small parts tray or on the load carrier such that all surfaces of the instruments are cleaned and disinfected.

2. Close WD and start the program, see the table below for the program sequence.

3. Remove the instruments at the end of the program.

4. Check that the load is dry and, if necessary, dry with medical compressed air.

5. Visual inspection for cleanliness is performed after removal from the WD. If contamination is still visible, re-clean medical devices again manually. Subsequently, the re-cleaned medical devices must again be reprocessed automatically.

MAINTENANCE, INSPECTION, AND CHECK:

| Equipment: Illuminated magnifying glass (3–6 dioptres).

All instruments must be inspected visually for cleanliness, integrity, and functionality, if necessary by using an illuminated magnifying glass (3–6 dioptres).

All instruments are to be checked for damage and wear. Damaged medical devices may no longer be used and must be sorted out.

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PACKAGING:

| Equipment: Film-paper packaging (e.g., steriCLIN, art. no 3FKB210112 and 3FKB210140), sealing device (e.g., HAWO, type 880 DC-V).

A suitable method (sterile barrier system) is to be used to package the instruments. Package according to DIN EN ISO 11607. A sterile barrier system (e.g., film-paper packaging) according to DIN EN ISO 11607 is to be used, which is intended for steam sterilization by the manufacturer. The instruments are double-packed. The packaging must be large enough to avoid stressing the sealing seam.

Note: After the heat sealing process, the sealing seam must be checked visually for any defects. In case of defects, the packaging must be opened and the instrument repacked and sealed.

STERILIZATION:

| Device: Sterilizer according to DIN EN 285 or small steam sterilizer according to DIN EN 13060, type B process. Process: Steam sterilization with fractionated pre-vacuum, 134 ºC, holding time minimum 3 minutes (in Germany according to KRINKO/BfArM recommendation 134 ºC minimum 5 minutes) or 132 ºC minimum 3 minutes (parameter of validation). Longer holding times are possible.

1. Place the packaged products in the sterilization chamber.

2. Start the program.

3. Remove the products at the end of the program and allow to cool down.

4. Then check the packaging for possible damage and screening effects. Faulted packaging must be regarded as being non-sterile. The instruments must be repacked and sterilized.

STORAGE:

| Duration of storage according to own specifications.

It is recommended to store instruments packed and protected from recontamination in proven suitable sterile packaging, cassettes, or retainers.

ADDITIONAL INFORMATION:| Disposal note: All polishers can be disposed of in the practice waste after a final sterilization cycle. A maximum of 2 reprocessing cycles including final sterilization is permitted.

MANUFACTURER CONTACT:

| EVE Ernst Vetter GmbH Neureutstr. 6

75210 Keltern, Germany

Telephone: +49 (0) 72 31 97 77 -0

Fax: +49 (0) 72 31 97 77 -99

E-Mail: info@eve-rotary.com www.eve- rotary.com

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