| Brand Name: | SHOMEA |
| Model Number: | OEM |
| MOQ: | 10pcs |
| Packaging Details: | Polybag, Carton, Wooden case or According to your request |
| Payment Terms: | L/C,D/A,D/P,T/T,Western Union |
Custom Machined Chiba Biopsy Needle Component for Image Guided Procedures - Built to Print
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Products Name |
Custom Machined Chiba Biopsy Needle Component for Image Guided Procedures - Built to Print |
| Material | Medical Grade Stainless Steel |
| Needle Type | Fine Puncture Needle |
| Needle Tip | Beveled Tip |
| Gauge | 18G–25G (Custom Available) |
| Length | 90–250 mm (Custom Available) |
| Connection | Luer Hub |
| OEM/ODM | Available |
| LOGO | Can be customized according to your drawing |
| Samples | Usually provide 5-10pcs samples for testing before mass production |
| Delivery Time | Usually 30-45 days or according to quantity |
Product Advantages:
Q1. What is a Chiba needle used for?
A: A Chiba needle is primarily used for fine needle aspiration (FNA), tissue biopsy, fluid aspiration, and image-guided interventional procedures.
Q2. What materials are used to manufacture the needle?
A: The needle is made from high-quality medical-grade stainless steel, providing excellent strength, corrosion resistance, and dimensional accuracy.
Q3. What sizes are available?
A: We offer a wide range of needle gauges and lengths. Custom specifications are available to meet different clinical and OEM requirements.
Q4. Is the product sterile and intended for single use?
A: No. Our products are non-sterile machined components, not finished or single-use medical devices.
Q5. Do you offer OEM and ODM services?
A: Yes. We provide OEM and ODM services, including customized needle dimensions, packaging, labeling, and private branding according to customer requirements.
Disclaimer
Shenzhen Shomea Hardware Products Co., Ltd. is a precision metal components manufacturer, not a medical device distributor. All parts shown on this page are custom machined according to the buyer's drawings, samples and specifications.
We do not sell finished medical devices, sterile devices, IVD reagents or surgical instruments. All components are supplied non-sterile and unfinished.
The purchaser, as the medical device manufacturer or equipment brand owner, is solely responsible for device design validation, biocompatibility evaluation, sterilization validation, labeling and regulatory approval of the finished medical device.