Import 500ml Pp Autoclaved Vaccine Bottle — Buy in wholesale FOB from Supplier in China

This 500ml PP autoclaved vaccine bottle is a sterile pharmaceutical container manufactured from medical-grade polypropylene for high-temperature and pressure sterilisation applications. The bottle carries CE, DMF and ISO certifications and offers a 500ml nominal capacity with uniform wall thickness throughout. Custom colours are available, with customer logo acceptance and customised printing options. The minimum order quantity is 1,000 pieces, packaged in standard export cartons or to buyer requirements.

The polypropylene material is selected for its thermal stability and compatibility with autoclave sterilisation cycles, as well as ethylene oxide (EO) sterilisation where required. Medical-grade PP resists deformation under repeated heat exposure and maintains dimensional integrity across standard autoclave parameters. The manufacturing takes place in a GMP-standard workshop with imported production equipment. Uniform wall thickness ensures consistent thermal transfer during sterilisation and reduces failure risk under vacuum or pressure differentials. The bottle is designed for compatibility with automated filling production lines.

This container suits vaccine manufacturers, biologics producers, and pharmaceutical compounders requiring sterile bulk storage or transport vessels. It is appropriate for cell culture media, buffer solutions, and active pharmaceutical ingredient intermediates. Buyers should confirm with Shijiazhuang Xinfuda whether the DMF filing covers the specific closure and seal configuration they require, as compatibility varies by stopper and cap combination. The supplier notes 20 years of product experience, though buyers should verify current GMP certification scope and recent audit status directly.

Shijiazhuang Xinfuda Medical Packaging Co., Ltd. is located at No. 269 Jianshe South Street, Shijiazhuang, Hebei Province, China, postal code 050000. The supplier holds a harbor trust tier on the platform, with a response rate of 0.00% and an average response time of 0 hours, indicating no recorded buyer engagement through this channel. Buyers should initiate direct contact to assess communication responsiveness and English-language capability before relying on platform messaging alone.

The listing emphasises 20 years of product experience, GMP-standard manufacturing, imported machinery, and a professional quality department. The company offers customisation of colour, logo, and printing. No information is provided about annual production capacity, specific pharmaceutical client references, FDA registration status, or EU regulatory compliance beyond the stated CE marking. Buyers should request a current quality agreement, audit report, and batch release documentation protocol. The DMF reference suggests US market intent, but the DMF number and holder status should be verified directly with the supplier and cross-checked with FDA Orange Book or DMF database records.