从China供应商批发进口15mm Flip Off Caps — FOB条款

Zibo Ruiyue Packaging Materials Co., Ltd., based in Shandong Province, China, manufactures these 15mm flip-off caps designed for pharmaceutical and injectable drug vial closures. The caps are constructed from an aluminium-plastic or aluminium-only composite, with a design that allows the plastic component to be removed easily by flipping, exposing the aluminium seal beneath without causing significant damage to the aluminium hole. This mechanism is standard in parenteral drug packaging, enabling needle access to the vial stopper while maintaining a tamper-evident seal.

Flip-off caps of this type are widely used in the pharmaceutical industry for sealing glass vials containing injectable solutions, vaccines, and lyophilised drugs. The 15mm size corresponds to the common 13mm and 20mm vial neck finishes used globally, and the aluminium-plastic construction provides both a sterile barrier and visual tamper evidence. Industry-standard flip-off caps typically comply with ISO 8362 or ISO 8536 series for injection vials and closures, though buyers should confirm the specific standards this product meets with the supplier.

These caps are purchased by pharmaceutical manufacturers, contract packaging companies, and medical supply distributors. Zibo Ruiyue states it holds ISO 9001 certification and describes itself as an experienced manufacturer of aluminium caps. Buyers should confirm the exact cap finish diameter, crimp compatibility with their vial specifications, and whether the supplier can provide certificates of conformity or extractable/leachable testing data for regulated pharmaceutical markets.

Zibo Ruiyue Packaging Materials Co., Ltd. is located at No. 128, Zhenxing Road, Yiyuan County, Zibo City, Shandong Province, China. The company identifies itself as an experienced manufacturer of aluminium caps, with a product focus on pharmaceutical closure solutions including flip-off caps. Its marketplace listing carries a harbour trust tier.

The supplier states it holds ISO 9001 quality management certification, which is a standard requirement for pharmaceutical packaging manufacturers. However, the listing does not provide details on GMP compliance, cleanroom production facilities, or specific pharmaceutical regulatory approvals such as US FDA Drug Master Files or EU TSE certificates. The response rate and average response time are currently listed at zero, so buyers should allow time for initial communication and request full documentation before engaging in procurement discussions.