仕様
| 項目 | 製品情報 |
|---|---|
| ゲージ | 32G / 34G |
| 長さ | 4 mm |
モデル・構成
| モデル | ゲージ | 長さ |
|---|---|---|
| 32G × 4 mm | 32G | 4 mm |
| 34G × 4 mm | 34G | 4 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。
Compact micro needles for professional aesthetic device portfolios. The supplied catalogue lists two fine-gauge configurations, 32G × 4 mm and 34G × 4 mm, with ODM support for configuration, branding and packaging.
Micro needle configurations
The catalogue presents two 4 mm reference configurations. The needle length remains the same, while the gauge differs.
| Configuration | Gauge | Needle length |
|---|---|---|
| 32G × 4 mm | 32G | 4 mm |
| 34G × 4 mm | 34G | 4 mm |
Product presentation
The brochure illustrates micro needle packaging and individual needle accessories. These products are presented alongside the cannula and multi-needle ranges as compact options within the professional precision-device collection.
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 ↗