
Breast Surgery Agris-Dingman Dissector – Set of 2 (Left & Right) – 36 cm
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Hospital & Volume Procurement Pricing
The Breast Surgery Agris-Dingman Dissector is a specialized surgical instrument designed for compatible breast surgery and plastic surgery applications. This product is supplied as a set of two instruments, consisting of one left configuration and one right configuration, with each instrument measuring 36 cm in length.
The paired left and right design provides complementary working orientations for procedures where access from different sides is required. The 36 cm length provides an extended working profile suitable for compatible surgical applications where additional reach may be beneficial.
Design and Configuration
The set contains two dissecting instruments:
- Left configuration – 36 cm
- Right configuration – 36 cm
The mirrored left and right configurations allow the instruments to be selected according to the required working orientation. Their dedicated design is intended to support controlled handling during compatible breast surgery procedures.
Breast Surgery Applications
The dissectors are designed for compatible breast and plastic surgery applications requiring a specialized dissecting instrument.
Potential applications include:
- Breast surgery
- Plastic surgery
- Reconstructive surgery
- Breast tissue dissection
- Surgical tissue handling
Specific applications depend on the procedure, surgical technique, and professional clinical judgment.
Handling and Use Considerations
The instruments should be handled carefully to preserve their working profiles and overall alignment. Before use, inspect the working end and shaft for visible damage, deformation, corrosion, or other conditions that could affect intended performance.
The appropriate left or right configuration should be selected according to the requirements of the procedure.
Cleaning and Instrument Care
After use, the dissectors should be cleaned according to the applicable validated surgical instrument-care protocol. Particular attention should be given to the working ends and any areas where surgical material may remain.
Proper handling and storage can help protect the 36 cm shaft and working surfaces from unnecessary damage.
Sterilization and Inspection
Where reusable processing is applicable, sterilization should follow the manufacturer's validated instructions and the healthcare facility's established sterilization protocol.
Before each use, inspect both instruments for cleanliness, alignment, surface condition, and overall mechanical integrity. Any damaged instrument should be evaluated according to the facility's instrument-management procedures.
Technical Specifications
| Specification | Details |
|---|---|
| Instrument Type | Breast Surgery Dissector |
| Configuration | Left & Right |
| Set Quantity | 2 Pieces |
| Length | 36 cm each |
| Surgical Specialty | Breast Surgery / Plastic Surgery |
| Application | Tissue Dissection / Surgical Handling |
| Product Type | Variable Product |
| Material | Not specified |
| Working-End Dimensions | Not specified |
| Sterilization | Follow applicable validated protocol |
Frequently Asked Questions
1. How many instruments are included?
The set contains two dissectors: one left and one right.
2. What is the length of each dissector?
Each instrument is 36 cm long.
3. Are left and right configurations included?
Yes. The set includes both left and right configurations.
4. What is the instrument designed for?
It is designed for compatible breast surgery and plastic surgery applications involving controlled dissection and tissue handling.
5. Can the instruments be purchased as different configurations?
The product is configured with separate Left and Right variations.
6. What material are the instruments made from?
The material has not been specified in the supplied product information.
7. Are the instruments reusable?
Reusability has not been explicitly specified. Processing and reuse should follow the manufacturer's validated instructions.
8. How should the dissectors be sterilized?
Sterilization should follow the manufacturer's validated instructions and the applicable healthcare facility protocol.
