What is the lead time for production?

Lead time is 1 to 3 months, depending on the season.

Does the machine support CIP/SIP functions?

Yes, the pump structure supports Clean-in-Place (CIP) and Sterilize-in-Place (SIP) functions.

GMP Approved Snuff Fluid Dispensing System Rhinitis Solution Packaging and Sealing Device

Name: GMP Approved Snuff Fluid Dispensing System Rhinitis Solution Packaging and Sealing Device
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2169879965

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$30,000.00-99,000.00

1 Piece

Product profile

After-sales Service

Engineers Available to Service Machinery Overseas, Online Support,video Technical Support

Certification

CE, GMP, ISO

Condition

New

Model NO.

Customized IVEN -1

Customized

Fill Range

1L & Above

Filling Principle

Gravity Filling

Main Material

Glass, Plastic, Stainless Steel

Voltage

380V

Warranty

1 Year

Pump Type

Ceramic Pump, Peristaltic Pump, Metal Pump

Process Type

Washing, Sterilizing, Filling, Stoppering, Capping

Industrial Use

HPLC, Uplc, LC, Gc, LC-Ms, Gc-Ms Analysis

Capacity

Customized

Filling Speed

3500-4000 Bottles/Hour

Bottle Height

Base on Actual Customization

Stable Production Capacity

30-250 Bottles/Minute

Bottle Moving Mode

Intermittent Type/ Rotary Type

Filling Range

5-500ml

Number of Filling Heads

2 Heads-24 Heads

Filling Accuracy

≤±0.5%

Transport Package

Carton; Wooden Case; Wooden Package;

Specification

9620.00cm * 2540.00cm * 2330.00cm

Trademark

IVEN

Origin

China

HS Code

8422303090

Production Capacity

Customized

Key features

GMP & CE Certified: Meets GMP requirements and holds CE, ISO certifications for pharmaceutical safety.

Flexible Customization: Offers full customization for pump type, process, capacity, and bottle dimensions.

High Speed Production: Stable production capacity ranges from 30 to 250 bottles per minute.

Advanced Automation: Features PLC control, servo motor driving, and automatic bottle unscrambling.

Anti-Leak Technology: Equipped with anti-leaking device for bottom filling to avoid bubbles.

CIP/SIP Support: Pump structure supports Clean-in-Place and Sterilize-in-Place functions.

Overseas Technical Support: Engineers available for overseas service, online support, and video technical assistance.

Company profile

Years of Export ExperienceLow MOQPatents AwardedProduct Certification

Shanghai Iven Pharmatech Engineering Co., Ltd.

Shanghai, China

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc. CertifiedExport Year: 19 Years CertifiedNearest Port: Shanghai PortAverage Response Time: ≤1.43h CertifiedTerms of Payment: LC, T/T, D/P, etc.

AI-Powered supplier vetting

SummaryThe supplier is a combined company offering pharmaceutical and medical production equipment, including vial, ampoule, prefilled syringe, oral liquid, tablet, capsule, visual inspection, packaging, and logistics solutions. It provides extensive customization and integrated services such as process design, equipment selection, installation, commissioning, and validation. Export activity is substantial, with 71%–90% of sales from exports and 19 years of export experience. Quality assurance, ISO9001:2015 certification, CE capability, manufacturing contracts, and finished-product inspection instructions are documented strengths. However, the supplier lacks in-stock, overseas warehouse, overseas showroom, overseas agent or branch capabilities, and has no written procedures for service assessment, corrective actions, or complaint handling. R&D evidence is limited: no SDK, no new products in the past year, and no ODM or major-brand OEM services. No specific customer cases are provided.

CertificationsThe supplier reports an ISO9001:2015 certificate and CE certification capability, providing explicit evidence of quality-management and product-compliance credentials. However, the slices do not specify the scope, validity period, or products covered by these credentials.

After-Sales capabilityThe supplier lists installation, commissioning, validation, maintenance, debugging, repair, training, and integrated consulting services, and provides equipment installation-related offerings. Nevertheless, it has no overseas agents or branches, no overseas warehouse or showroom, and no written procedures or records for complaint handling, service assessment, or corrective and preventive actions, indicating an operational weakness in documented after-sales management.

R&D capabilityThe supplier has customization-oriented R&D services, but reports no available SDK, no new products during the past year, no ODM service, and no OEM service for popular brands. These explicit limitations indicate weak evidence of current product innovation and platform development.

Production capacityThe supplier covers multiple pharmaceutical equipment production lines, including vial and ampoule, prefilled syringe and cartridge, oral liquid, tablet and capsule, inspection, packaging, and logistics systems. It has valid manufacturing contracts with each affiliated subcontractor, follows finished-product inspection instructions uniformly, and reports quality assurance, although no quantitative production-capacity data is provided.

Customization capabilityThe supplier explicitly offers customization from samples, designs, full customization, minor customization, and flexible customization. Its integrated solution includes process design, conceptual and construction design, equipment selection, model customization, installation, commissioning, and validation, demonstrating broad customization coverage.