Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
The 3M ESPE D82229 RotoMix Capsule Mixing Unit is a dental laboratory mixing device designed for mixing compatible encapsulated dental materials. Its rotating mixing mechanism provides a consistent mixing motion for material preparation in dental and laboratory environments. Operating on a 120V power supply at 60Hz, the RotoMix unit features a dedicated capsule mixing configuration suitable for compatible dental material preparation workflows.
Specifications:
Brand: 3M
Model: D82229
Product Line: RotoMix
Product Type: Capsule Mixing Unit
Equipment Type: Dental Mixing Equipment
Mixing Type: Rotational Mixing
Voltage: 120V
Frequency: 60Hz
Function: Capsule Material Mixing
Application: Dental Material Preparation
Features:
RotoMix capsule mixing design
Rotational mixing mechanism
Designed for compatible dental material capsules
Dedicated dental mixing equipment configuration
Suitable for dental laboratory workflows
Technical Details
| Brand | 3M |
|---|---|
| Category | Capsule Mixing Unit |
| Medical Discipline | General Surgery |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | 3M |
| SKU | DA42-ITEM-R |
| Warranty | 30 - Warranty |
Need This Product Certified Patient-Ready?
If you require this product to be patient-ready certified, you can request a quote. Inspection, testing, repair, electrical safety testing, and calibration services are available through A Biomedical Service, Inc.
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No similar items available.
Safety & Biomedical Inspection Notice
Shipping & Receiving Notice
Medical equipment may require inspection, functional verification, calibration, preventive maintenance, safety testing, or other evaluations following transportation and before being placed into service.
Upon receipt, the purchaser is responsible for inspecting the equipment for any shipping damage and determining whether any inspection, testing, calibration, preventive maintenance, or certification is necessary based on the manufacturer's recommendations, the receiving facility's policies, and all applicable laws and regulations.
The equipment should not be placed into clinical service or used for patient care until the purchaser has verified that it is safe, appropriate, and compliant for its intended use.
Biomedical Inspection Notice
Medical equipment should be evaluated by qualified personnel before being placed into clinical service. Depending on the type of equipment, the evaluation may include, as applicable:
- Electrical safety testing
- Functional performance verification
- Alarm verification (if applicable)
- Battery inspection or replacement (if applicable)
- Calibration verification (if applicable)
- Preventive maintenance
- Software configuration and system settings
- Verification of compatible accessories, consumables, and disposables
- Inspection for shipping or handling damage
- Compliance with the manufacturer's recommendations
- Compliance with the receiving facility's policies, procedures, and applicable regulatory requirements
Transportation, storage, handling, and installation may affect the performance of medical equipment. Reuse Medical recommends that the receiving facility inspect, test, and evaluate the equipment in accordance with the manufacturer's recommendations and the facility's biomedical engineering procedures before placing the equipment into clinical service or patient use.
