Kids E-Dental E-MTA (Mineral Trioxide Aggregate)

A bioactive tricalcium silicate cement for vital pulp therapy, perforation repair, root-end procedures, and selected regenerative endodontic applications.

₹3,000.00
SKU
12-585
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Description

Successful endodontic treatment depends on accurate diagnosis, appropriate case selection, careful technique, and the correct use of a suitable repair material. Kids E-Dental E-MTA is a tricalcium silicate-based bioactive cement developed for vital pulp therapy, endodontic repair, and selected regenerative procedures in primary and permanent teeth.

The material is supplied as an ultrafine, hydrophilic powder intended to provide a smoother and more manageable consistency during mixing and placement. Its bioactive behaviour is designed to support mineral deposition and the biological response associated with repair when the material is used in contact with suitable tissue fluids.

Available product information describes the cement as having high alkalinity, low solubility, strong radiopacity, and washout resistance. These characteristics are relevant in procedures where adaptation, placement stability, and postoperative radiographic assessment are important. Material stability and adaptation are clinically significant, although treatment success still depends on diagnosis, isolation, operator technique, moisture control, and the complete restorative or endodontic protocol.

The manufacturer describes the formulation as quick setting, which may help streamline the clinical workflow when used according to the current instructions. Exact working time and setting time should be confirmed from the current manufacturer Instructions for Use because mixing consistency, temperature, moisture, and placement conditions may affect performance.

The kit includes both liquid and gel components. The liquid is intended to produce a more granular or sand-like mix, while the gel produces a thicker, putty-like consistency. This allows the clinician to select a handling profile suited to the procedure, subject to the manufacturer’s current protocol.

Kids E-Dental E-MTA is indicated for selected procedures including pulp capping, pulpotomy, perforation repair, resorption repair, root-end filling, regenerative endodontics, and selected root repair procedures. It should be used only for indications supported by the current manufacturer instructions and with appropriate case selection.

Key Features
  • Tricalcium silicate-based bioactive endodontic cement.
  • Ultrafine hydrophilic powder for smoother mixing and placement.
  • Designed to support mineral deposition and dentinal bridge formation.
  • Manufacturer-reported high alkalinity.
  • Manufacturer-reported low solubility.
  • Manufacturer-reported washout resistance.
  • High radiopacity supports postoperative radiographic assessment.
  • Liquid and gel components provide different handling consistencies.
  • Suitable for selected procedures in primary and permanent teeth.
  • Airtight tube presentation supports controlled dispensing and storage.
  • Manufacturer describes the material as quick setting.
  • Intended for professional dental use only.
Packaging

Contents:

  • 8 × 1 g Airtight Powder Tubes
  • 1 × 2 ml Liquid
  • 1 × 2 ml Gel
Specification
Specification Details
Brand Kids E-Dental
Product Name E-MTA (Mineral Trioxide Aggregate)
Product Type Bioactive Endodontic Cement
Principal Material Tricalcium Silicate-Based Cement
Powder Characteristics Ultrafine, Hydrophilic
Setting Characteristics Reported as Quick Setting by Manufacturer
Reported Properties Bioactive, Washout Resistant, Low Solubility
Radiopacity Reported as High
Mixing Components Powder with Supplied Liquid or Gel
Suitable For Primary and Permanent Teeth
Clinical Applications Vital Pulp Therapy and Endodontic Repair
Professional Use Yes
Manufacturer Kids E-Dental LLP
Directions to use
  1. Prepare the treatment site according to the planned procedure and establish appropriate isolation.
  2. Dispense the required amount of powder onto a clean glass slab or mixing pad.
  3. Select the supplied liquid or gel according to the consistency required for the clinical procedure.
  4. Mix the powder with the selected liquid or gel in the ratio and for the duration specified in the current manufacturer instructions. Available product information reports an approximate 3:1 powder-to-liquid ratio and about 30 seconds of mixing.
  5. Use the mixed material immediately to reduce the risk of dehydration.
  6. Carry the material to the prepared site using an MTA carrier or another suitable placement instrument.
  7. Adapt the material gently using an appropriate instrument. Use moisture control or a damp cotton pellet only when required by the selected procedure and the current manufacturer protocol.
  8. Inspect the placement clinically and radiographically where appropriate.
  9. Complete the coronal seal or restoration according to the planned treatment protocol.
  10. Dispose of unused mixed material and clean the mixing instruments according to standard clinical procedures.

For professional dental use only. Refer to the current manufacturer Instructions for Use for exact timings, ratios, moisture requirements, and setting conditions.

Additional Information

Clinical Considerations

  • Intended for professional dental use only.
  • Accurate diagnosis, case selection, isolation, and placement technique remain essential.
  • Do not allow the mixed material to dehydrate before placement.
  • The liquid and gel produce different handling consistencies; select the component according to the procedure and current manufacturer guidance.
  • Do not assume that one consistency is appropriate for every indication.
  • Avoid overfilling or extrusion beyond the intended treatment site.
  • Control contamination before and during placement.
  • Radiographic review may assist with evaluation of placement where clinically relevant.
  • The final coronal seal and restorative protection remain important to treatment success.
  • Exact working time, setting time, moisture requirements, and restoration timing should follow the current IFU.
  • The manufacturer describes the material as washout resistant, but performance still depends on correct mixing, placement, and moisture control.

Cleaning and Material Handling

  • Use a clean glass slab or mixing pad and clean instruments for each procedure.
  • Avoid contamination of the powder, liquid, gel, and dispensing openings.
  • Do not return dispensed powder or liquid to the original container.
  • Clean reusable placement instruments immediately after use before the material hardens.
  • Follow the instrument manufacturer’s validated cleaning and sterilisation instructions.
  • Dispose of single-use applicators and contaminated material according to local clinical-waste requirements.

Storage and Handling

  • Store in the original packaging in a dry environment.
  • Protect the powder from moisture contamination.
  • Replace the cap immediately after dispensing.
  • Keep the liquid and gel containers tightly closed.
  • Protect the material from excessive heat and direct light.
  • Do not use after the expiry date printed on the packaging.
  • Record the batch number where clinical traceability is required.
  • Dispose of contaminated or unused mixed material according to local regulations.

Manufacturer

Manufacturer: Kids E-Dental LLP

Manufacturer
Brand Kids E-Dental
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Frequently Asked Questions

It is intended for selected vital pulp therapy, pulp capping, pulpotomy, perforation repair, resorption repair, root-end filling, and regenerative endodontic procedures.
It is a tricalcium silicate-based bioactive Mineral Trioxide Aggregate cement.
Yes. The manufacturer lists indications in both primary and permanent dentition, subject to appropriate case selection and the current IFU.
It is designed to release calcium-containing species and support mineral deposition in contact with tissue fluids. The clinical response depends on correct case selection, handling, and placement.
The liquid is intended to provide a more granular or sand-like mix, while the gel produces a thicker, putty-like consistency for selected procedures.
The manufacturer describes the formulation as washout resistant. Performance still depends on correct mixing, placement, moisture control, and the clinical environment.
The manufacturer describes the material as highly radiopaque, supporting postoperative radiographic assessment. An exact radiopacity value was not provided in the supplied information.
Available product information reports an approximate 3:1 powder-to-liquid ratio, but the current manufacturer IFU should be followed for the selected liquid or gel and intended procedure.
Retailer and manufacturer-supplied product information commonly reports approximately 30 seconds. Confirm the current mixing time in the manufacturer IFU before use.
The manufacturer describes the formulation as quick setting. Refer to the current IFU for the exact setting time and conditions, as temperature, moisture, and consistency may affect performance.
Yes. Root-end filling is listed among the manufacturer-supported indications for permanent teeth.
No. The material forms one part of the procedure. Isolation, correct placement, moisture control, and a suitable final coronal seal or restoration are also important.
Keep it in its original packaging in a dry place, protect the powder from moisture, and reseal all containers immediately after dispensing.
Yes. It should be used only by qualified dental professionals following the current manufacturer Instructions for Use.

More Information

More Information
Brand Kids E-Dental
Packaging

Contents:

  • 8 × 1 g Airtight Powder Tubes
  • 1 × 2 ml Liquid
  • 1 × 2 ml Gel

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