规格参数
| 项目 | 产品信息 |
|---|---|
| 配置数量 | 8 |
| 针规 | 18G–30G |
| 长度 | 25–70 mm |
| 外径 | 0.3–1.2 mm |
型号与配置
| 针规 | 长度 | 外径 |
|---|---|---|
| 18G | 70 mm | 1.2 mm |
| 21G | 50 mm | 0.8 mm |
| 22G | 50 mm | 0.7 mm |
| 23G | 50 mm | 0.6 mm |
| 23G | 70 mm | 0.6 mm |
| 25G | 50 mm | 0.5 mm |
| 27G | 40 mm | 0.4 mm |
| 30G | 25 mm | 0.3 mm |
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。
The ES Cannula range offers eight blunt-tip cannula reference configurations, with gauges from 18G to 30G, lengths from 25 mm to 70 mm and listed outer diameters from 0.3 mm to 1.2 mm. The portfolio supports specification selection and ODM configuration.
Complete cannula size reference
Each row identifies a specific gauge, length and diameter combination from the ES Cannula range. Two 23G options are listed, with lengths of 50 mm and 70 mm.
| Gauge | Length | Outer diameter |
|---|---|---|
| 18G | 70 mm | 1.2 mm |
| 21G | 50 mm | 0.8 mm |
| 22G | 50 mm | 0.7 mm |
| 23G | 50 mm | 0.6 mm |
| 23G | 70 mm | 0.6 mm |
| 25G | 50 mm | 0.5 mm |
| 27G | 40 mm | 0.4 mm |
| 30G | 25 mm | 0.3 mm |
Specification selection
Select the reference configuration by its gauge, length and outer diameter. The listed dimensions are product-selection references; clinical instructions follow the applicable manufacturer IFU.
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
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alexmoon@ictmedicalco.com ↗