你们可以为医疗设备加工组件吗?
GPT Precision 审核用于设备外壳的 CNC 加工咨询, structural components, 安装零件, mechanical interfaces and development fixtures. 可行性和供应范围取决于图纸, 材料, 预期应用和项目要求.
开发原型可以用于成品医疗设备吗?
开发样品是为特定评估目的制造的. The responsible device team determines suitability for finished-device use through the relevant validation and approval process.
How should we specify materials and surface treatments?
Provide the material grade, 状态, surface finish and applicable specifications. Identify special contact, cleanliness or sterilization-related requirements for manufacturing scope review.
Are inspection reports and material certificates included?
Identify the inspection reports, material certificates and traceability records you need during the inquiry so availability and scope can be confirmed.
How are quotation and production lead times determined?
Quotation timing is assessed after reviewing the inquiry. Production lead time depends on drawings, materials, quantity and the agreed manufacturing scope, and is confirmed during quotation or order review.