MD-Guidewire Spring
Fine spring families for guidewire and interventional device component review.
For guidewire, MDI, nasal spray and medical device component programs, AUKIN pairs 0.02mm-level precision capability with ISO 13485 documentation and batch traceability.

Philippine pharmaceutical manufacturers, medical device assemblers and CDMO teams often need more than a small spring sample. They need clean processing, material clarity, traceable inspection and files that can move through QA without being rebuilt from scratch.
Fine spring families for guidewire and interventional device component review.
Small compression springs for metered-dose inhaler and regulated valve applications.
Micro spring options for nasal spray pump and pharmaceutical dispenser programs.
Micro-coil capability for projects where wire size and batch stability are critical.
| Item | AUKIN capability | Buyer value |
|---|---|---|
| Wire range | Down to 0.02mm | Supports micro spring review before scaling to trial production. |
| Quality system | ISO 13485:2016 certified medical QMS | Relevant for regulated medical component supplier approval. |
| Process | Cleanroom process and Japanese ITAYA precision machines | Designed for clean, controlled micro spring production. |
| Documentation | PPAP / APQP and batch traceability available | Helps QA teams check material, process and inspection evidence. |
| Proof image | 0.06mm wire / 0.34mm OD guidewire sample shown in site material | Gives technical buyers an immediate sense of micro-scale capability. |
Medical device quality management certificate for strict compliance programs.
Useful for medical spring review where contamination control matters.
Inspection and production records can be reviewed before supplier approval.
Include wire diameter, OD, free length, load points, material and documentation expectations.