| Brand Name: | NA |
| Model Number: | OEM |
| MOQ: | Based on customer requirements |
| Price: | NA |
| Packaging Details: | Polybag, Carton, Wooden case or According to your request |
| Payment Terms: | L/C,D/A,D/P,T/T,Western Union |
| Products Name | Custom Machined Pen Tip Side Hole Needle Component with Luer Connector - Built to Print |
|---|---|
| Material | Stainless Steel, Brass, Aluminum, brass, copper ,etc |
| Surface treatment | Sandblasting, polishing, knurling, laser marking, etc |
| Tube Outer Diameter | 0.25-15mm |
| Tube wall Thickness | 0.05-3mm |
| Meta Base | Male and Female thread |
| Tolerance | OD/ID±0.02mm L±0.05mm or According to Drawing |
| Size | 3G-32G or Customized |
| LOGO | Can be customized according to your drawing |
| Samples | Usually provide 5-10pcs samples for testing before mass production |
| Delivery Time | Usually 25-30 days or according to quantity |
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Q1: What luer types can you match for this side hole pen tip needle?
A1: We can make male or female luer connectors according to your technical requirements.
Q2: Can we customize side hole position and hole size?
A2: Yes, side hole location, aperture and needle geometry can be produced from your drawings.
Q3: Are these needles supplied sterile?
A3: No. All our needles are supplied non-sterile as machined components. We are a precision metal components manufacturer, not a sterile device supplier.
Q4: What material options are available?
A4: Medical grade 304 /316 stainless steel are available, alternative alloys can be customized.
Q5: Is sample validation supported before bulk order?
A5: Yes, custom samples are available for function testing before mass production.
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.