What are the power specifications?

The power is 2.4kW, 380V 50Hz, with an output power range of 10kV~35 kV and frequency range of 500Hz~50kHz.

Is customization available for this machine?

Yes, the machine is customized and offers full customization options for specific needs.

What is the minimum order quantity?

The minimum order quantity is 1 set.

Wholesale Customization Injectable Ampoule Automatic Leak Testing Machine

Name: Wholesale Customization Injectable Ampoule Automatic Leak Testing Machine
Brand: Hunan Zhengzhong Pharmaceutical Machinery Co., Ltd.
SKU: 2014463805

Hunan, ChinaHunan Zhengzhong Pharmaceutical Machinery Co., Ltd.

US$100,000.00-200,000.00

1 Piece

Product profile

Customization

Available

After-sales Service

Online Support, video Technical Support

Analysis Speed

High Throughput

Model NO.

JAZ

Application

Pharmaceutical Industry

Certification

CE, GMP, ISO

Condition

New

Customized

Detection Range

Small Molecules

Material Compatibility

Liquid

Portability

Benchtop

Power Source

Electric Operated

Sensitivity

High Sensitivity

Technology

Ultraviolet-Visible Spectroscopy

User Interface

Software Interface

Voltage

380V

Type

Medicine Detecting Instrument

Finished Dosage Form

Liquid

Precision

High Precision

Computerized

Warranty

2 Year

Transport Package

Nude

Specification

Huge

Trademark

Z-Zone

Origin

China

Key features

High Efficiency Inspection: Capacity of 300-400 bottles/min with automatic online inspection capabilities.

High Accuracy Detection: Detects superfine cracks and pinholes that traditional methods miss.

Non-Destructive Testing: Inspects containers without side effects or damage to the product.

Versatile Application: Inspects ampoules and vials by simply changing the mold.

GMP Compliance: Provides full validation criteria to meet strict GMP requirements.

Patented Technology: Holds 17 authorized invention and utility model patents.

Advanced Control System: Features a friendly touch screen for control, display, and data collection.

No Pollution Risk: Electrodes and liquid do not directly contact, ensuring product safety.

Company profile

High Repeat Buyers ChoiceImporters and ExportersExhibition ExperienceFull Customization

Hunan Zhengzhong Pharmaceutical Machinery Co., Ltd.

Hunan, China

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available CertifiedCustomization Options: Full Customization CertifiedExport Year: 4 Years CertifiedNearest Port: Shenzhen PortAverage Response Time: ≤24h

AI-Powered supplier vetting

SummaryThe supplier operates in electromechanical equipment, pharmaceutical machinery, food-safety testing products, software, and related services. It reports a 42,000 m² facility, more than 200 employees, 10 production lines, and 41–50 quality-control staff, but its stated primary export market is domestic. Quality procedures, complaint handling, corrective actions, and supplier assessment procedures are documented and followed. The supplier holds ISO9001:2015 certification and reports prior ISO9001:2008 certification, but lacks a factory environmental impact assessment report. It provides ODM services and SDK availability, while reporting no new products in the past year and no OEM service for popular brands. It has no in-stock capacity, overseas warehouse, overseas showroom, or valid manufacturing-capacity contract with related subcontractors. Financial evidence is inconsistent and indicates zero values for several latest-year metrics; therefore, financial credibility cannot be confirmed. No customer cases...

Supplier typeThe supplier is a manufacturer and developer of electromechanical and pharmaceutical machinery, food-safety testing products, mechanical parts, integrated electrical systems, and software. Its reported facility, workforce, and production lines support classification as a manufacturing-oriented supplier rather than only a trading intermediary.

CertificationsThe supplier reports ISO9001:2015 certification and previously passed ISO9001:2008 certification, as well as historical national quality-mark certification. However, it reports no factory environmental impact assessment report, so certification coverage is positive for quality management but incomplete for environmental compliance.

After-Sales capabilityThe supplier has documented and followed procedures for corrective and preventive actions, customer complaints, and supplier service-capability assessment. However, it reports no in-stock service capacity, overseas warehouse, or overseas showroom, which limits service infrastructure; overall capability is supported but not comprehensive.

Production capacityThe supplier reports a 42,000 m² facility, more than 200 employees, 10 production lines, and 41–50 quality-control staff, with peak-season lead time of 4–6 months and off-season lead time of 2–3 months. These details support established production capacity, although the supplier reports no inventory capability and no valid manufacturing-capacity contract with related subcontractors.

Customization capabilityThe supplier’s business scope includes research and development, software development, system integration, and mechanical parts processing. It explicitly provides ODM services and has an available SDK, supporting customization and technical integration; no evidence is provided for OEM service to popular brands.

Product Q&A

Q:What types of products can this machine inspect?

It is dedicated to inspecting ampoules, vials, and oral liquid products for liquid leakage, pinholes, and cracks.

Q:What is the inspection capacity of the machine?

The machine has a capacity of 300-400 bottles per minute.

Q:Is the inspection process non-destructive?

Yes, it achieves non-destructive inspection. Products are loaded with low energy for a short time and insulated during inspection, causing no side effects.

Q:Can this machine handle different container sizes?

Yes, it is versatile and can inspect different container sizes, such as ampoules and vials, by changing the mold.

Q:Does the machine meet GMP requirements?

Yes, it provides a full set of validation criteria to meet GMP requirements.