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Vial Filling Machine
Created with Pixso. Aseptic Gravimetric Powder Filling Machine for 10ml Vials Closed-Loop Dosing Precision and Moisture Control for High-Value Active Pharmaceutical Ingredients

Aseptic Gravimetric Powder Filling Machine for 10ml Vials Closed-Loop Dosing Precision and Moisture Control for High-Value Active Pharmaceutical Ingredients

Brand Name: Lingyao
Model Number: LYKFG2-30F
MOQ: 1 unit
Price: 150,000-400,000USD per piece
Delivery Time: 180 work days
Payment Terms: D/A,D/P,T/T,Western Union
Detail Information
Place of Origin:
China(Thailand available soon)
Certification:
CE, ISO, GMP
Machine Name:
Powder Filling Machine
Availavle Vials Size:
10ml
Output Capacity:
30-50 BPM
Vials Material:
Glass
Breakage Rate:
<0.5%
Material Compatibility:
SS316
After-sales Service & Technical Support:
2 Years Guarantee Maintenance, Free Spare Parts Available, And Trouble Assistance To Minimize Downtime
Plugging Style:
Full
LAF System:
ISO Class 5(Optional)
Packaging Details:
carton, wood carton, pallets
Supply Ability:
4 pc per 6 months
Highlight:

Vial Filling Machine

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Powder Filling Sealing Machine

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Powder Filling Machine

Product Description

Aseptic Gravimetric Powder Filling Machine for 10ml Vials

Closed-Loop Dosing Precision and Moisture Control for High-Value Active Pharmaceutical Ingredients

Product Overview

In the processing of highly potent, moisture-sensitive powder formulations and advanced active pharmaceutical ingredients (APIs), the margin for volumetric error is zero. The Lingyao Aseptic Powder Filling Machine is an elite, pilot-to-clinical scale automation platform engineered specifically for 10ml (2R-20mm neck) tubular glass vials.

Operating at a highly controlled, precise output of 30 to 50 Vials Per Minute (BPM), this unit completely abandons outdated volumetric augers in favor of advanced Closed-Loop Gravimetric Dosing. Enclosed within an ISO Class 5 Laminar Airflow (LAF) environment, the machine integrates dynamic nitrogen purging and high-resolution optical inspections, guaranteeing a dosing accuracy of ≤ ±1% (for 0.5g to 3g ranges) while maintaining absolute batch sterility.

The Cause: Powder Caking, Density Drift, and Particulate Contamination

Handling hygroscopic or ultra-fine pharmaceutical powders introduces severe operational bottlenecks that traditional liquid-filling architectures cannot resolve:

  1. Powder Density Variations: Traditional volumetric auger fillers assume the powder density remains constant. However, vibration and settling alter the powder matrix during a production run. This density drift results in catastrophic weight variations, leading to rejected batches of extremely expensive APIs.

  2. Hygroscopic Caking: Sensitive lyophilized powders rapidly absorb ambient humidity. If exposed to standard atmospheric air during the dosing phase, the powder cakes and clumps, clogging the dispensing nozzles and ruining the formulation's solubility.

  3. Invisible Contaminants: Glass shards or foreign fibers inside an empty vial can easily go unnoticed by human operators. If a particulate is buried under 3 grams of opaque powder, visual inspection at the end of the line is impossible, exposing the manufacturer to severe regulatory recalls.

The Solution: Automated Optical Inspection and Gravimetric Feedback

The Lingyao engineering team resolved these complex powder-handling vulnerabilities through real-time mass verification and strict environmental controls.

To conquer density drift, the fluid pathway utilizes an advanced Gravimetric Load Cell Architecture. Instead of measuring volume, the machine weighs every individual vial before and immediately after dosing. This closed-loop feedback instantly micro-adjusts the dispensing auger in real-time, locking the final fill weight to an exact ≤ ±1% tolerance. To prevent bridging and caking, the powder hopper features a patented anti-vibration agitator combined with a continuous Dry Nitrogen Purge, ensuring residual moisture remains strictly ≤0.5%.

To guarantee particulate-free operations, the infeed track incorporates an Automated Optical Inspection (AOI) Station. High-speed CMOS cameras scan the interior of every empty vial to detect particulates down to 50μm. Any contaminated vial is automatically rejected before it ever reaches the expensive powder dosing station, significantly reducing API waste.

Technical Specifications

Core Performance Parameter Technical Data Specification
Applicable Container Format 10ml Tubular Glass Vials (2R-20mm Crimp Neck)
Production Speed Capacity 30 - 50 Vials / minute (Adjustable for settling time)
Target Dosing Range 0.5g - 3.0g
Gravimetric Dosing Precision ≤ ±1% Deviation (Self-Calibrating Load Cells)
Moisture Control System Integrated Dry N₂ Purge (Reduces consumption by up to 40%)
Pre-Fill Quality Control AOI Machine Vision (≤50μm Particulate Detection)
Environmental Protection HEPA-Filtered Laminar Airflow (ISO Class 5 / Zone A)
Data Compliance Architecture FDA 21 CFR Part 11 Ready (Audit Trails & E-Signatures)
Total Electrical Power Approx. 3.0 KW (380V, 50Hz)

Aseptic Gravimetric Powder Filling Machine </p>
<p><img src=Targeted Industrial Applications

  • Clinical Trial Batches (Phase I/II): Highly precise, small-batch processing for expensive, newly synthesized powder APIs requiring meticulous weight verification.

  • Specialized Lyophilized Formulations: End-to-end integration capabilities for workflows requiring precise dry-powder dispensing following bulk freeze-drying processes.

  • Agile R&D and Orphan Drugs: Programmable PLC interfaces allow rapid parameter changeovers, making it the perfect asset for high-mix, low-volume production facilities.

Turnkey Global Compliance and Regional Deployment

Deploying an aseptic powder line requires an equipment partner capable of delivering flawless validation documentation. Engineered through our versatile TachoCraft Thailand manufacturing base, Lingyao equipment is constructed from premium AISI 316L stainless steel (contact parts) to sustain demanding compliance audits worldwide.

The machine’s HMI is fully equipped to generate encrypted electronic batch records, ensuring immediate compliance with global traceability mandates. We accompany your asset with comprehensive engineering services, providing complete IQ/OQ/PQ validation dossiers and expert on-site commissioning. This rigorous technical support drastically expedites SABER/SASO customs clearances across the Middle East and ensures seamless regulatory approvals in expanding North American and European markets.