ICT MEDICAL
专业产品系列

4 mm精细针头

Micro Needles

所提供系列列出两种微针规格:32G × 4 mm及34G × 4 mm。两者长度同为4 mm,针规不同。

Micro Needles — 4 mm精细针头

规格参数

项目产品信息
针规32G / 34G
长度4 mm

型号与配置

型号针规长度
32G × 4 mm32G4 mm
34G × 4 mm34G4 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。

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.

ConfigurationGaugeNeedle length
32G × 4 mm32G4 mm
34G × 4 mm34G4 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.

StepFocusDetails
01 / SelectReference models and desired specificationsChoose the product family and reference configurations for the intended portfolio.
02 / CustomizeConfigurations, labels and packagingDefine the configuration, label and packaging requirements.
03 / DocumentTechnical files and applicable credentialsPrepare the technical documentation and applicable credential information.
04 / ReviewSampling, approval and order conditionsReview 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 portfolioScope described in the brochure
CEDevice- and model-specific applicability.
ISO 13485Manufacturer quality management system.
GMPManufacturing quality controls.

专业业务咨询

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alexmoon@ictmedicalco.com ↗
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