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Wire Mesh Machine for Pharmaceutical Industry With Mill Test Report
Product Spotlights
GMP-compliant wire mesh machines with full material traceability via Mill Test Reports. Features precision tension control for pharmaceutical-grade filtration mesh. Built with FDA-approved materials and global certifications including ISO9001/14000. Modular design enables rapid changeovers between 2-500 mesh configurations. Global service network supports operations across 5 continents.
Negotiable
MOQ: 1 Piece (Price negotiable depending on order volume and customization)
Key Specifications
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Material:
Stainless Steel 304/316
Wire Diameter Range:
0.02mm - 5.0mm
Mesh Count Range:
2 - 500 mesh/inch
Payment & Shipping
Payment Methods:
Port of Shipment:
China
Delivery Detail:
Delivery time depends on order quantity.
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Material
Stainless Steel 304/316
Wire Diameter Range
0.02mm - 5.0mm
Mesh Count Range
2 - 500 mesh/inch
Control System
PLC Automation
Application
Pharmaceutical Filtration
Certifications
ISO9001, ISO14000, OHSAS18001
Machine Type
Automatic Weaving
Brand
Anping Kexing
Function
Precision Woven Wire Mesh
As a trusted manufacturer from Anping Kexing Wire Mesh Manufacturing Co., Ltd. in Hengshui, China, we specialize in delivering precision wire mesh machines engineered for the stringent requirements of the pharmaceutical industry. Our equipment combines advanced automation with pharmaceutical-grade materials to ensure unparalleled mesh consistency and quality control. Each machine comes with a mandatory Mill Test Report (MTR) to provide full material traceability – a critical requirement for GMP compliance.
Key Technical Specifications:
| Parameter | Specification |
| Machine Type | Automatic High-Speed Weaving |
| Max Production Speed | 15 meters/minute |
| Tension Control Accuracy | ±0.1N |
| Power Requirements | 380V/50Hz (Customizable) |
Critical Advantages for Pharmaceutical Clients:
- Dual-stage filtration verification system ensures zero contamination risk
- All contact parts manufactured from FDA-compliant materials
- Integrated quality monitoring with real-time defect detection
- Modular design allows quick changeover between mesh configurations
Why Partner With Us?
With certifications including ISO9001, ISO14000, and OHSAS18001, our manufacturing processes meet global pharmaceutical standards. Our machines serve clients across 5 continents including North America, Western Europe, and Southeast Asia – testament to their reliability in diverse operational environments. The included MTR documentation provides:
- Full material chemical composition analysis
- Mechanical property verification
- Heat treatment certification
- Third-party validation stamps
Frequently Asked Questions:
-
Q: Are your machines validated for cleanroom use?
A: Yes, our standard models meet ISO Class 7 requirements with optional upgrades for higher classifications. -
Q: Can you provide material certification for FDA submissions?
A: Our MTR packages include all necessary documentation for regulatory filings. -
Q: What maintenance support do you offer globally?
A: We provide remote diagnostics and have service partners in all major markets including North America and Europe. -
Q: How does the MTR ensure traceability?
A: Each report contains unique heat numbers linking materials to specific production batches. -
Q: Can machines handle specialty alloys like Hastelloy?
A: Yes, our tension systems accommodate exotic alloys upon request. -
Q: What's your lead time for customized configurations?
A: Standard units ship in 30 days with custom projects requiring 60-90 days.
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Product Certifications
HACCP, TL900, QS9000, SA8000, ISO9001, ISO9004, ISO17799, ISO9000, ISO14000, ISO10441, ISO16949, TS16969, ISO19011:2000, OHSAS18001, Others
Main Markets
North America, South America, Eastern Europe, Southeast Asia, Africa, Oceania, Mid East, Eastern Asia, Western Europe, Central America, Northern Europe, Southern Europe, South Asia, Domestic Market
Location
Hengshui, Hebei, China
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