仕様
| 項目 | 製品情報 |
|---|---|
| 構成数 | 8 |
| ゲージ | 18G–30G |
| 長さ | 25–70 mm |
| 外径 | 0.3–1.2 mm |
モデル・構成
| ゲージ | 長さ | 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・技術資料
提供資料のODMプロセスは、参照モデルの選択、構成・ラベル・包装のカスタマイズ、技術文書の準備、サンプル・承認・発注条件の確認という流れです。
MYTHCOの2024年資料にはCE、ISO 13485、GMPのマークが表示されています。CEの適用は機器・モデルごとに異なり、ISO 13485はメーカーの品質管理システム、GMPは製造品質管理に関するものです。
英語原文の詳細情報
以下に製品ガイドの英語原文を保持しています。上記の翻訳概要・仕様表は資料を構造的に整理したもので、PDFはメーカーまたは提供元の原本です。
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. |
業務に関するお問い合わせ
会社名、仕向国、希望モデル、数量をご記入ください。メールアプリが開きます。お問い合わせが自動送信・保存されることはありません。
alexmoon@ictmedicalco.com ↗