What is the lead time for production?

The lead time is 1-3 months during peak season and one month during the off-season.

Does the machine include a SCADA system?

Yes, it features a computer-based SCADA system that records data and complies with GAMP regulations.

What is the drying capacity range?

The drying capacity ranges from 20 Liters to 150 Liters depending on the model selected.

CIP-SIP Freeze Dryer Pharmaceutical Freeze Drying Machine

Name: CIP-SIP Freeze Dryer Pharmaceutical Freeze Drying Machine
Brand: Zhejiang Lyomac Pharmaceutical Equipment Co., Ltd.
SKU: 885613535

Zhejiang, ChinaZhejiang Lyomac Pharmaceutical Equipment Co., Ltd.

US$7,000.00-12,000.00

1 Piece

Sample price:US$12000.00/piece.Request sample

Product profile

Customization

Available

Certification

CE, GMP, ISO, Usfda, Eugmp, cGMP

Condition

New

Customized

Voltage

as Customer Require

Drying Capacity

40 Liter

Shelf Area

3.24 M2

Shelf Size(LWH)

900*600*20mm

Usable Shelf No.

Vial Loading Quantity

7500-14000

Installation Dimension(LWH)

4000*1500*2200mm

Weight

4500kg

Power

28 Kw

Finished Dosage Form

Liquid

Precision

High Precision

Computerized

Warranty

1 Year

Type

Sterile Liquid, Diagnosis Material Freeze Drying

Transport Package

Standard Seaworthy and Land Transportation Packing

Specification

LYOPRO-3.0

Trademark

Lyomac

Origin

Shanghai

HS Code

8419399090

Production Capacity

1set /Quarter

Key features

Customized Design: Fully customizable voltage, drying capacity, and shelf configurations to meet specific needs.

CIP/SIP System: Integrated Cleaning-in-Place and Sterilization-in-Place systems for pharmaceutical compliance.

High Precision Control: SCADA system with GAMP regulation compliance, ensuring precise temperature and vacuum control.

Compact & Flexible: Compact design with flexible arrangement to save space and suit various plant layouts.

Multi-Model Range: Available in 5 models with drying capacities ranging from 20 to 150 Liters.

GMP & FDA Compliant: Designed to comply with cGMP, FDA, CE, ISO, and other international pharmaceutical standards.

Easy Operation: Simple operation suitable for R&D, with no utility requirements apart from power supply.

Company profile

Zhejiang Lyomac Pharmaceutical Equipment Co., Ltd.

Zhejiang, China

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Customization from Samples CertifiedExport Year: 7 Years CertifiedNearest Port: Shanghai Port, Ningbo PortAverage Response Time: ≤24h

AI-Powered supplier vetting

SummaryThe supplier is a China-based limited company offering vacuum freeze dryers. Evidence identifies Zhejiang Lyomac Pharmaceutical Equipment Co., Ltd., established in 2018, with 14 employees in one record and 17 in another. It holds an ISO9001:2015 certificate, while another description also references TUV-CE and ISO9001 certification. The supplier reports private mold design, 3D software design, SDK availability, professional technical supplier status, and sample-based customization. Manufacturing contracts with associated subcontractors are in place, and more than 10 production lines are reported, although lead-time information is inconsistent. Overseas services include installation, debugging, training, and repair. Documented procedures exist for supplier assessment, corrective actions, and complaints, but records are absent. Financial-period data is provided, but no financial figures or explicit financial assessment are available. No customer cases, inventory capability, overseas warehouse, or showroom...

Supplier typeThe supplier is identified as a limited company from China, offering vacuum freeze dryers. It is reported as independent of a larger company group, although the records show different employee counts and locations.

CertificationsThe supplier explicitly reports an ISO9001:2015 certificate, and its company description additionally references TUV-CE and ISO9001:2000 certification. These statements support established quality-system certification, though the validity and scope of the additional certifications are not independently documented.

After-Sales capabilityOverseas services include equipment installation, debugging, training, and repair, and a valid manufacturing contract exists with each associated subcontractor. However, service-management, corrective-action, and complaint procedures have no written records; the supplier also reports no overseas warehouse or showroom.

Production capacityThe supplier reports more than 10 production lines, valid manufacturing contracts with associated subcontractors, and broad international export markets. Capacity assessment is constrained by inconsistent lead-time records: one source states 4–6 months off-season, while another states one month off-season and gives an unclear peak-season entry.

Customization capabilityThe supplier explicitly provides customization from samples and reports private mold design and 3D software design services. These statements directly support the ability to develop customized products based on customer samples.