Injectable Vial Washing-Drying&Sterilization-Powder Filling&Pluging-Cap Sealing IV Fluid Machine

Name: Injectable Vial Washing-Drying&Sterilization-Powder Filling&Pluging-Cap Sealing IV Fluid Machine
Brand: CHINNOFI PHARMACEUTICAL MACHINERY CO., LTD.
SKU: 716821152

Jiangsu, ChinaCHINNOFI PHARMACEUTICAL MACHINERY CO., LTD.

US$30,000.00-90,000.00

1 Piece

Product profile

Customization

Available

After-sales Service

24 Hours on Line

Certification

CE, GMP, ISO

Condition

New

Customized

Voltage

380V

Warranty

2 Year

Capacity

2000-6000vials/Hour as Per Urs

Filling Dosage

0.5g-2g 2g-10g, 10g-30g, 20g-50g

Type

Pharmaceutical Packaging Machinery

Precision

High Precision

Computerized

Finished Dosage Form

Powder

Transport Package

Woodencase

Specification

2ml-1000ml vials

Trademark

CHINNOFI

Origin

China

HS Code

8422301090

Production Capacity

2000-6000vials/Hour as Per Requirements

Company profile

Importers and ExportersHigh Repeat Buyers ChoiceExperienced TeamExhibition Experience

CHINNOFI PHARMACEUTICAL MACHINERY CO., LTD.

Jiangsu, China

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.