ANRITSU CORPORATION Pharmaceutical Business Div. Infivis Company Official site

Aerosol CanCheckweigher

Assuring Aesol Can Quality

<Features> ■ Maximum sorting accuracy ±0.01g ■ Stable handling for high qccuracy ■ Simple interface and reliable operation checks ■ Compliant with FDA 21 CFR Part 11(optional) *For more details, please refer to the related links or feel free to contact us.

Related Link - https://www.anritsu.com/ja-jp/product-inspection/p…

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KW9627AP00

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KW9627AP00

Aerosol Can Checkweigher KW9627AP00

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[Trusted Worldwide: Anritsu Inspection Systems] Anritsu inspection systems are used globally to ensure product safety and quality across a wide range of industries and applications. Key Features of Our Weighing & Inspection Solutions ●Contaminant Detection  Detects foreign materials such as metal, bone, glass, ceramic, and more. ●Content Verification  Checks for missing or excess items, presence/absence, and item counts. ●Package Inspection  Identifies issues like product caught in seals and defective printing. ●Weight Inspection  Performs quantitative checks and grading for consistent product quality. ●Production & Quality Management  Enables centralized control, real-time monitoring, statistical analysis, and traceability through our proprietary system, QUICCA. [Supporting the Pharmaceutical Industry Since 1964] Anritsu delivered its first checkweigher to a pharmaceutical manufacturer in 1964. Inspired by the industry's strict standards for quality control, we have continuously evolved our technologies to meet advanced quality assurance needs. Today, Anritsu Infivis works closely with pharmaceutical partners to address complex challenges in manufacturing and compliance. [In-House Development for Superior Performance] All Anritsu products—including weighcells—are developed in-house. This commitment to innovation is reflected in the high performance of our electromagnetic force balance weighcells. [Enhancing Quality and Productivity in Pharma] Anritsu’s inspection technologies contribute to improved quality and efficiency in pharmaceutical manufacturing and R&D environments.