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High-Precision Amber Vial Filling and Stoppering Machine for Pharmaceuticals
Negotiable
1 Piece
Product profile
Customization
AvailableCertification
CE, GMP, ISOCondition
NewModel NO.
DYGDCustomized
CustomizedVoltage
380VWarranty
1 YearSuitable Bottle
50ml-100ml, 100ml-500ml, 500ml-1000mlCapacity
60-120 Bottles/Min Based on 50mlElectrical Supply
380V 50/60HzPower Consumption
1.2kwFilling Heads
4Tolerance of Filling
≤±1%Vacuum
0.066MPa, 20m3 /HCompressed Air
0.4-0.6 MPa, 25-35L/MinSingle Machine Noise
≤60 dBWeight
~1000kgOverall Dimensions
1400×1200×1600mmType
Pharmaceutical Packaging MachineryFinished Dosage Form
LiquidPrecision
High PrecisionComputerized
ComputerizedTransport Package
Wooden CaseSpecification
2ml, 10ml-100ml 100ml-1000mlTrademark
CHINNOFIOrigin
ChinaProduction Capacity
50 Sets/YearCompany profile
Business Type: Manufacturer/FactoryExport Year: 2016-10-18Average Response Time: ≤4.78hTerms of Payment: LC, T/TInternational Commercial Terms(Incoterms): FOB, CIF
AI-Powered supplier vetting
SummaryThe supplier is a limited trading company with 11 employees, offering pharmaceutical, food-processing, and chemical equipment, including reactors, filling machines, autoclaves, water systems, dryers, and packaging lines. It reports ISO 9001 and GMP certification, available SDK support, R&D and customization capabilities, new product launches during the past year, and extensive export coverage. R&D engineer experience is reported at 41–50 years in aggregate, with 21–30 quality-control staff and an off-peak lead time of 2–3 months. Service infrastructure includes overseas agents or branches, an overseas showroom, and participation in the CPHI trade show. Financial records are indicated for 2020–2022, but no financial performance values are provided. Supplier service procedures exist, although the assessment procedure has no records. Raw-material traceability and several sustainability controls remain unknown. No specific customer cases are provided.
CertificationsThe supplier reports holding ISO 9001 and GMP certifications. These are explicit quality and manufacturing-system credentials relevant to its equipment scope.
After-Sales capabilityThe supplier reports 15 qualified service-capability suppliers, a corrective and preventive action procedure with follow-up records, overseas agents or branches, an overseas showroom, and service coverage in Europe and America. However, the service-capability assessment procedure has written procedures but no records, limiting verification depth.
R&D capabilityThe supplier reports an available SDK, new products launched during the past year, customization from samples and designs, and total R&D engineer experience of 41–50 years. These points explicitly support established innovation and development capability.
Production capacityThe supplier states that it manufactures general equipment and pharmaceutical, food-processing, and chemical equipment, with a broad product range, 21–30 quality-control staff, and a reported off-peak lead time of 2–3 months. An audit was conducted by BV, but the audit result is recorded as 0 without an explanatory interpretation, so production-system performance cannot be fully assessed.
Customization capabilityThe supplier explicitly offers customization from samples and customization from designs. This directly demonstrates both sample-based and design-based customization services.
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*To:
CHINNOFI PHARMACEUTICAL MACHINERY CO., LTD.
CHINNOFI PHARMACEUTICAL MACHINERY CO., LTD.*Content:
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