Specifications
| Parameter | Product information |
|---|---|
| Gauge | 32G |
| Pin count | 9 |
| Source dimensional designation | 0–1.5 mm |
Technical reference
Do not interpret 0–1.5 mm as a universally confirmed operating setting. Check the selected version’s exact dimensional definition and compatibility information.
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.
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. |
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 ↗