规格参数
| 项目 | 产品信息 |
|---|---|
| 针规 | 32G |
| 针数 | 9 |
| 来源尺寸标注 | 0–1.5 mm |
技术参考
请勿把0–1.5 mm解读为所有版本通用且已确认的操作设置。应核对所选版本的确切尺寸定义及兼容性信息。
ODM 与技术文件
所提供系列描述ODM流程：选择参考型号；定制配置、标签与包装；准备技术文件；随后审核样品、批准事项及订单条件。
MYTHCO 2024来源目录展示CE、ISO 13485及GMP标志。CE适用范围取决于具体器械及型号；ISO 13485指制造商质量管理体系，GMP指生产质量控制。
完整英文原始详情
下方保留产品指南的完整英文文本。上方本地化介绍及规格表是对资料的结构化整理；PDF 保留制造商或来源的原始文件。
A screw-type multi-needle accessory presented with nine pins and a 32G specification. The catalogue carries the dimensional designation 0–1.5 mm and illustrates the accessory and its product packaging.
Product reference
The nine-pin accessory is shown in the catalogue as part of the micro-delivery range. Its three printed reference specifications are 32G, 9 pins and 0–1.5 mm.
| Reference parameter | Catalogue specification |
|---|---|
| Gauge | 32G |
| Number of pins | 9 |
| Format | Screw-type multi needle |
| Source dimensional designation | 0–1.5 mm |
Version-specific dimensional information
The 0–1.5 mm value is reproduced as the manufacturer-source designation. The brochure states that its exact dimensional definition and packaging depend on the selected version.
ODM configuration and branding
ODM support is available for product configuration, branding and packaging. AB LIFE GLOBAL presents a four-step process, from selecting reference models to reviewing samples and order conditions.
| Step | Focus | Details |
|---|---|---|
| 01 / Select | Reference models and desired specifications | Choose the product family and reference configurations for the intended portfolio. |
| 02 / Customize | Configurations, labels and packaging | Define the configuration, label and packaging requirements. |
| 03 / Document | Technical files and applicable credentials | Prepare the technical documentation and applicable credential information. |
| 04 / Review | Sampling, approval and order conditions | Review samples, approvals and order conditions. |
Manufacturer-source portfolio credentials
The 2024 MYTHCO source portfolio displays CE, ISO 13485 and GMP marks. The brochure presents these as manufacturer-supplied portfolio credentials, with CE applicability determined by the particular device and model.
| Mark displayed in the source portfolio | Scope described in the brochure |
|---|---|
| CE | Device- and model-specific applicability. |
| ISO 13485 | Manufacturer quality management system. |
| GMP | Manufacturing quality controls. |
专业业务咨询
请注明公司、目的国、所选型号及数量。此操作将打开邮件应用，不会自动发送或保存咨询。
alexmoon@ictmedicalco.com ↗