
Ophthalmology Atkinson Retrobulbar Needle 23g
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The Ophthalmic Atkinson Retrobulbar Needle is a specialized ophthalmic instrument featuring a 23G needle configuration. It is designed for compatible ophthalmic applications requiring an Atkinson-style retrobulbar needle.
The fine 23G configuration provides a defined needle profile for appropriate ophthalmic instrument setups. The supplied product information does not specify the overall needle length, tip configuration, material, or hub design.
Design and Configuration
The instrument is configured as an Atkinson Retrobulbar Needle with a 23G gauge. The Atkinson configuration identifies the supplied needle style, while the 23G specification defines the needle gauge.
Additional specifications such as shaft length, tip geometry, hub configuration, and material have not been provided and are therefore not assumed.
Ophthalmic Application
The needle is designed for compatible ophthalmic applications where an appropriately configured retrobulbar needle is required.
Potential applications include:
- Ophthalmic surgery
- Eye surgery
- Ophthalmic anesthesia-related instrument setups
- Retrobulbar needle applications
- Professional ophthalmic clinical environments
Specific clinical use should be determined by a qualified ophthalmic professional according to the procedure and applicable clinical protocols.
23G Configuration
The 23G specification provides a fine-gauge needle configuration. This fixed gauge is the primary sizing characteristic supplied for the product.
The exact needle length and tip design should be confirmed from the manufacturer's product specifications where required.
Handling and Use Considerations
The needle should be handled carefully to protect the needle shaft and tip from bending or other damage. Before use, inspect the instrument for visible deformation, contamination, damage, or other abnormalities.
Use should follow applicable professional ophthalmic protocols and manufacturer instructions.
Cleaning and Instrument Care
If the product is intended for reusable processing, cleaning should follow the manufacturer's validated instructions and applicable healthcare-facility protocols.
If supplied as a single-use product, it should be managed according to the manufacturer's labeling and applicable medical-device procedures. Reusability has not been specified in the supplied information.
Sterilization and Inspection
Sterilization requirements depend on the product configuration and manufacturer's validated instructions. The appropriate processing method should be confirmed from the applicable product documentation.
Before use, inspect the needle for tip integrity, shaft condition, cleanliness, and overall structural integrity.
Technical Specifications
| Specification | Details |
|---|---|
| Instrument Type | Atkinson Retrobulbar Needle |
| Surgical Specialty | Ophthalmology |
| Gauge | 23G |
| Configuration | Atkinson / Retrobulbar |
| Application | Ophthalmic Surgery |
| Working Profile | Fine-Gauge Needle |
| Product Type | Simple Product |
| Overall Length | Not specified |
| Needle Length | Not specified |
| Tip Configuration | Not specified |
| Material | Not specified |
| Hub Configuration | Not specified |
| Sterilization | Follow applicable validated protocol |
Frequently Asked Questions
1. What gauge is the Atkinson Retrobulbar Needle?
The needle is 23G.
2. What type of needle is this?
It is an Atkinson Retrobulbar Needle designed for compatible ophthalmic applications.
3. What is the instrument designed for?
It is designed for compatible ophthalmic applications requiring a specialized retrobulbar needle.
4. Is the needle length specified?
No. The overall needle length has not been provided.
5. What is the tip configuration?
The supplied product information does not specify the tip configuration.
6. What material is the needle made from?
The material has not been specified.
7. Is this a variable product?
No. Based on the fixed 23G specification, it is treated as a Simple Product.
8. Is it reusable?
Reusability has not been explicitly specified. Processing or disposal should follow the manufacturer's validated instructions and labeling.
