Stable Low Residue Error Alarm High Efficiency Capsule Filler Machine

Name: Stable Low Residue Error Alarm High Efficiency Capsule Filler Machine
Brand: Jining Factop International Trade Co., Ltd.
SKU: 2165159802

Shandong, ChinaJining Factop International Trade Co., Ltd.

US$10,000.00

1 Piece

Product profile

Customization

Available

After-sales Service

Online Support,video Technical Support

Certification

CE, GMP, ISO

Model NO.

NJP1200C

Condition

New

Customized

Fill Range

≤49ml

Filling Principle

Volumetric Filling

Machine Type

Capsule Filling Machine

Main Material

Stainless Steel

Voltage

380V

Warranty

1 Year

Weight

1000 Kg

Total Power

5.5kw

Vacuum

40m3/H-0.04-0.08MPa

Operating Noise

<75db(a)

Filling Capacity

72000 PCS Per Hour

Transport Package

Wooden Packing

Specification

1100×910×2100 mm

Trademark

Origin

China

Key features

High Efficiency Filling: Capacity up to 38000 pcs/hour with 99% filling accuracy.

GMP Compliant Design: Manufactured with full stainless steel structure meeting GMP standards.

Automatic Die Cleaning: Integrated mechanism removes residual powder to prevent cross-contamination.

Anti-Bridging Hopper: Large-capacity hopper ensures uniform powder feeding and minimizes segregation.

Vacuum Separation: Vacuum-assisted mechanism ensures accurate capsule body and cap separation.

Customizable Configuration: Non-standard customization available for capacity, voltage, and workshop size.

One-Year Warranty: 12 months free warranty covering whole machine excluding consumables.

Overseas Support: Includes installation, commissioning, training, and lifelong technical support.

Company profile

Importers and ExportersHigh Repeat Buyers ChoiceFast DeliveryMinor Customization

Jining Factop International Trade Co., Ltd.

Shandong, China

Business Type: Manufacturer/Factory, Trading CompanyExport Year: 2014-06-20Nearest Port: Shanghai, NingboAverage Response Time: ≤0.62hTerms of Payment: T/T, Western Union, Money GramInternational Commercial Terms(Incoterms): FOB, EXW, CFR, CIF, DDP, DAP, FCA

AI-Powered supplier vetting

SummaryThe supplier manufactures pharmaceutical and packaging machinery, including blister packing, sugar coating, tablet counting, and related production equipment. Its products are exported to the United States, Europe, the Middle East, Southeast Asia, and North America, with exports representing 51%–70% of total sales and eight years of exporting experience. Production and delivery indicators are partially positive, including peak- and off-season lead times within 15 workdays and stated quality assurance with raw-material traceability. However, the supplier has no documented corrective-action or complaint-handling procedures, no supplier-service assessment records, no listed management-system certification, no overseas service infrastructure, no inventory service capability, and no new products launched during the previous year. R&D and design resources appear limited, with one R&D engineer and minor customization capability. Customer retention is reported at 50%–80%, but specific customer cases are not provided.

Supplier typeThe supplier is a manufacturer and developer of pharmaceutical production and packaging machinery, including blister packing, sugar coating, tablet counting, and powder-to-tablet/capsule equipment. It sells domestically and exports to the United States, Europe, the Middle East, Southeast Asia, and North America, with eight years of export experience and stated self-operated import/export rights.

CertificationsThe supplier states that its tablet-press digital control system supports alignment with cGMP and FDA requirements, but the available information does not identify a certification held by the supplier. Supplier management-system certification is explicitly listed as NIL, so no formal certification holding is evidenced.

After-Sales capabilityThe supplier cites good after-sales service as a company tenet and accepts multiple quotation terms, but it has no written corrective/preventive-action procedures, no written customer-complaint procedures or records, and no written service-capability assessment procedure. It also reports no overseas agents or branches, overseas warehouse, showroom, inventory capability, or overseas service countries, indicating limited documented and local service infrastructure.

R&D capabilityThe supplier reports integrated development and production capabilities and describes high-tech machinery development, but it has only one R&D engineer, one year of total R&D-engineer experience is reported, and no new products were launched during the previous year. These explicit indicators show limited recent innovation output.

Production capacityThe supplier reports integrated manufacturing of several pharmaceutical machinery categories, exports representing 51%–70% of sales, annual production output above the stated threshold, and lead times within 15 workdays in both peak and off-season periods. Quality assurance and raw-material traceability are reported, although finished products are randomly inspected and checked by packing staff, which limits the evidence of a robust final-inspection system.

Customization capabilityThe supplier explicitly offers minor customization. No evidence is provided of moderate or extensive engineering customization, so the demonstrated capability is limited to minor modifications.

Product Q&A

Q:What pharmaceutical equipment does your company mainly produce?

We professionally design and manufacture tablet press machines, capsule filling machines, softgel encapsulation machines, bottle packaging production lines, and blister packaging machines. We also provide turnkey projects for solid dosage form complete production lines.

Q:Do you have fully automatic models? Can the machine be customized?

We have semi-automatic and fully automatic standard models. Non-standard customization is available according to production capacity, raw material, workshop size, and voltage configuration to meet different pharmaceutical factory requirements.

Q:Are your company machines GMP compliant? Can you provide certification documents?

All our pharmaceutical machines are manufactured in strict accordance with GMP standards with full stainless steel structure. We can provide machine drawings, compliance documents, and factory test reports to support project acceptance.

Q:Can you provide overseas installation, commissioning, and after-sales service?

We provide overseas installation, commissioning, and operator training, as well as lifelong technical support. The machine enjoys one-year warranty, and spare parts are supplied permanently.

Q:What is the after-sales service policy for your equipment?

Warranty: 12 months free warranty for the whole machine (excluding consumables). Free repair and parts replacement for non-human-induced failures during warranty.