A.O. Type 2.0mm External Fixator for Radius & Ulna – Surgical Instrument
Direct Manufacturer Pricing • Tax Exclusive
The A.O. Type 2.0mm External Fixator for Radius and Ulna is an orthopedic fixation device intended for external stabilization of selected forearm fractures. Designed for radius and ulna applications, this system requires confirmation of its component compatibility, configuration, and manufacturer specifications before clinical use.
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Hospital & Volume Procurement Pricing
The A.O. Type 2.0mm External Fixator for Radius and Ulna is an orthopedic fixation product intended for external stabilization of selected fractures involving the forearm bones. The radius and ulna work together to support forearm movement and function, making appropriate fracture stabilization an important consideration in orthopedic treatment.
External fixation systems generally use fixation elements connected to an external support structure to help maintain bone alignment. The specific configuration, indications, and fixation capabilities of this 2.0mm system depend on its design and the manufacturer's instructions.
The designation “A.O. Type” identifies the stated style of the product; it should not be interpreted as proof of manufacture, approval, or endorsement by AO Foundation or another organization. Buyers should verify the manufacturer, product documentation, and compatibility requirements before purchase.
Design and Features
This product is identified as a 2.0mm external fixator for radius and ulna applications. The listed measurement may relate to a particular component or system specification; the product title does not clarify its exact meaning.
External fixation systems may incorporate bone fixation elements, connecting components, and an external support structure. However, the precise components supplied with this product, their dimensions, and their connection design are not specified in the title. Confirm the complete configuration with the supplier.
Compatibility between fixation components is essential. Verify the intended bone application, component interfaces, available sizes, and any required accessories before combining this product with other orthopedic instruments or fixation devices.
Intended Orthopedic Applications
External fixation is used in selected orthopedic cases to support fracture stabilization. Depending on the system design and clinical indication, fixation may be considered for certain fractures involving the radius and ulna.
The suitability of this particular 2.0mm system depends on factors such as fracture characteristics, patient anatomy, bone quality, component design, and the treating surgeon's assessment. Its exact indications and limitations must be confirmed using the manufacturer's instructions for use.
Handling and System Selection
Choosing an external fixation system requires careful evaluation of the fracture pattern, required fixation configuration, component dimensions, and compatibility with the intended procedure.
Before use, inspect all supplied components for damage, deformation, corrosion, or manufacturing defects. Confirm that the parts connect correctly and comply with the manufacturer's assembly and handling instructions. Do not combine components from different systems unless compatibility is explicitly confirmed by the manufacturer.
The device should be selected, assembled, and applied by appropriately qualified healthcare professionals according to the approved instructions and clinical requirements.
Material, Cleaning, and Sterilization
The product title does not specify the material composition, sterile status, or reusable or single-use classification of this external fixator. Request these details from the supplier before purchase.
If the system or its components are supplied as reusable, follow the manufacturer's validated instructions for cleaning, inspection, sterilization, maintenance, and storage. Sterile and non-sterile products must be handled according to their labeling and applicable healthcare protocols. Do not assume that a specific sterilization method is appropriate without checking the instructions for use.
Choosing the Right External Fixator
When selecting an external fixator for the radius and ulna, verify the intended anatomical application, fixation element dimensions, system configuration, and compatibility with any required accessories.
The 2.0mm designation should be checked against the manufacturer's technical documentation to establish which component or dimension it describes. Confirming the complete specification helps ensure that the selected system meets the procedural requirements and is compatible with the intended fixation approach.
Key Features
AO-type external fixation system
Intended for radius and ulna applications
Listed 2.0mm size designation
Designed for selected orthopedic fracture stabilization applications
External fixation configuration, subject to manufacturer specifications
Exact included components not specified in the product title
Component compatibility should be verified before use
Material composition not specified
Sterile status and reusability must be confirmed
Intended use must follow the manufacturer's instructions
Product Specifications
| Specification | Details |
|---|---|
| Product Name | A.O. Type External Fixator for Radius & Ulna |
| Product Category | Orthopedic fixation device |
| Fixation Type | External fixation |
| Listed Size | 2.0mm |
| Intended Anatomical Area | Radius and ulna |
| Application | Selected forearm fracture stabilization |
| System Configuration | Confirm with supplier |
| Included Components | Not specified |
| Material | Not specified |
| Sterile Status | Confirm with supplier |
| Reusable or Single-Use | Confirm with supplier |
| Component Compatibility | Verify with manufacturer |
| Manufacturer | Not specified |
| Model Number | Not provided |
Frequently Asked Questions
1. What is an AO-type external fixator for the radius and ulna?
It is an external fixation product identified for applications involving the two bones of the forearm. The exact configuration and indications depend on the specific manufacturer's design.
2. What does the 2.0mm designation mean?
The product title lists 2.0mm, but it does not identify which component or dimension this measurement describes. Confirm the meaning in the manufacturer's technical specifications.
3. What is an external fixator used for?
External fixation systems are used in selected orthopedic cases to help stabilize fractures and maintain bone alignment. The appropriate system depends on the injury and the treating surgeon's assessment.
4. Can this system be used for both the radius and ulna?
The product title identifies both bones as intended anatomical areas. Confirm the precise indications and configuration with the manufacturer before clinical use.
5. What components are included?
The supplied title does not provide an itemized component list. Ask the supplier to confirm the included fixation elements, connecting components, external support structure, and any required accessories.
6. What material is the external fixator made from?
The material composition is not specified in the title. Request the manufacturer's material information and relevant product documentation.
7. Is the external fixator supplied sterile?
Sterile status is not stated. Confirm the packaging, labeling, and sterilization status with the supplier before use.
8. Can components from different external fixation systems be combined?
Only when the manufacturer explicitly confirms compatibility. Differences in dimensions and connection mechanisms can affect proper assembly and system performance.
9. Who should apply this external fixator?
Selection and application should be performed by appropriately qualified orthopedic professionals in accordance with the manufacturer's instructions and the patient's clinical needs.
10. What should I verify before purchasing?
Confirm the exact meaning of the 2.0mm designation, included components, material, sterile status, intended indications, compatibility requirements, and manufacturer documentation.