Specifications
| Parameter | Product information |
|---|---|
| Configurations | 8 |
| Gauge | 18G–30G |
| Length | 25–70 mm |
| Outer diameter | 0.3–1.2 mm |
Models and configurations
| 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 |
ODM and documentation
The supplied portfolio offers an ODM process: select reference models; customize configurations, labels and packaging; prepare technical documentation; then review samples, approvals and order conditions.
The 2024 MYTHCO source portfolio displays CE, ISO 13485 and GMP marks. CE applicability is device/model-specific; ISO 13485 refers to the manufacturer’s quality-management system, and GMP to manufacturing quality controls.
Complete English source detail
The complete English product-guide text is retained below. The localized overview and specification tables above are a structured adaptation; the PDF remains the original manufacturer/source document.
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. |
Professional enquiry
Include your company, destination country, selected model and required quantity. This opens your email application; it does not send or store an enquiry automatically.
alexmoon@ictmedicalco.com ↗