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Durable Euro Cap Infusion Cap - 39mm Diameter for Syringe Models
US$0.05
600,000-5,999,999 Pieces
US$0.03
6,000,000+ Pieces
Sample price:US$0.00/piece.Request sample
Product profile
Capacity
16-39mmClosure Type
Pull-Ring Euro CapColor
White or TransparentModel NO.
Euro Cap 39G-3Material
PP/PE/TPENeck Finish
16-39mmSpecial Feature
Good SealingUsage
Infusion PharmaceuticalsModel No.
Euro CapDiameter
39mmType
SyringeSterilization
Ready to UseTransport Package
Two-Layer Low Density Polyethylene BagsSpecification
16-39mm PP/PE/TPETrademark
JSDOrigin
ChinaProduction Capacity
1000000/DayKey features
Zero Leakage & No Particle Shedding: Engineered with JSD131 elastomer to ensure zero leakage during needle withdrawal and no particle shedding during puncture.
BFS & FFS Compatible: Fully compatible with Blow-Fill-Seal and Form-Fill-Seal infusion filling lines for large-volume parenteral products.
Global Quality Compliance: Meets USP, EP, JP, ChP, ISO 15759, and ISO 8871-5 standards with ISO 15378 certification.
Easy Production Line Switch: Can replace combination caps of the same dimensions without any adjustments to existing production lines.
Customizable Sterilization: Sterilization temperature and duration can be increased according to specific customer requirements.
High-Purity Material: Manufactured from premium TPE/PP/PE materials with higher material purity compared to traditional rubber stoppers.
GMP Compliant Manufacturing: Produced in C+A grade cleanroom environments with fully automated feeding and visual inspection systems.
Company profile
Business Type: Manufacturer/Factory CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc. CertifiedExport Year: 1 Years CertifiedNearest Port: Shanghai PortAverage Response Time: ≤6.28h CertifiedTerms of Payment: T/T
AI-Powered supplier vetting
SummaryThe supplier demonstrates documented product-quality commitments, including conformity with USP, EP, JP, ISO, and CHP requirements, an ISO 15378-compliant quality system, finished-product inspection instructions, quality assurance, and raw-material traceability. It operates two production lines, reports inventory capability, and has valid manufacturing contracts with associated subcontractors. Customization is available across samples, designs, full, minor, and flexible requirements. However, evidence indicates limited international service reach, no overseas agents, branches, warehouses, or showrooms, and only one year of export experience. R&D capability appears limited: no new products in the past year, no ODM, SDK, or 3D design services, and only one year of R&D engineer experience. Formal supplier-service, corrective-action, and complaint-handling procedures are absent or undocumented. No customer cases or named brand OEM experience are provided.
Supplier typeThe supplier explicitly identifies itself as not being a professional technical supplier and does not provide 3D software design, ODM, SDK, or popular-brand OEM services. Its described offering is therefore oriented toward manufacturing and customization rather than advanced technical or branded OEM support.
After-Sales capabilityThe supplier reports in-stock service capability and accepts FOB and T/T terms, but has no overseas warehouse, showroom, agents, branches, or offline trade-show participation. Complaint handling and corrective/preventive action lack written procedures or records, indicating a documented after-sales-service weakness.
R&D capabilityThe supplier reports only one year of total R&D engineer experience, no new products in the past year, no ODM service, no SDK, and no 3D software design service. These explicit limitations indicate weak demonstrated innovation capability.
Production capacityThe supplier operates two production lines, has valid manufacturing contracts with associated subcontractors, reports inventory capability, and uses uniform finished-product inspection instructions. It also lists ten qualified service-capability suppliers, but its service-capability assessment lacks written procedures and approved-supplier records.
Customization capabilityThe supplier explicitly offers customization from samples, customization from designs, full customization, minor customization, and flexible customization. This is direct evidence of broad customization coverage, although no 3D software design service is available.
Product Q&A
Q:Are JSD Caps compatible with BFS infusion packaging?
A:
Yes, JSD Caps are specifically designed for BFS (Blow-Fill-Seal) and FFS (Form-Fill-Seal) systems. They ensure high sterility, minimal impurities, and stability of liquid medications in ISO Class A environments.
Q:Do I need to modify my production line to use JSD Caps?
A:
No, manufacturers can replace combination caps with JSD Caps of the same dimensions without making any adjustments to the production line. End users can also continue using the products in the same way.
Q:What certifications do JSD Caps meet?
A:
JSD Caps are compliant with ISO 15759 and ISO 8871-5 standards. The company holds ISO 15378 certification, and all products meet major global pharmaceutical standards including USP, EP, JP, and ChP.
Q:What materials are used to manufacture JSD Caps?
A:
JSD Caps are made from premium TPE, PP, or PE materials. They utilize a proprietary JSD131 elastomer and advanced multi-material co-injection molding technology for optimal performance.
Q:Why are Euro Caps preferred over thermoset rubber combination caps?
A:
Thermoset rubber combination caps carry higher risks of chemical and particulate contamination due to carcinogenic accelerators and antioxidants. Euro Caps offer a safer alternative with better regulatory alignment for modern pharmaceutical standards.
Send Inquiry
*To:
Shanghai JSD New Medical Material Co., Ltd
Shanghai JSD New Medical Material Co., Ltd*Content:
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