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Top Quality G 1.5% Peritoneal Dialysis Solution 2000ml-Huaren Pharmaceutical
US$2.50-4.50
100 Pieces
Sample price:US$0.00/piece.Request sample
Product profile
Customization
AvailableApplication
Hematological SystemUsage Mode
Abdominal UseSuitable for
Elderly, Children, AdultState
LiquidShape
LiquidType
Inorganic ChemicalsPharmaceutical Technology
Chemical SynthesisDrug Reg./Approval No.
H20113088Validity Period
24 MonthsTransport Package
CartonSpecification
2000ml: 1.5% glucoseTrademark
HuarenOrigin
Qingdao, Shandong, ChinaProduction Capacity
10000000pieces/YearKey features
Clinical Indication: Suitable for acute and chronic renal failure patients requiring peritoneal dialysis.
Composition Details: Contains Glucose, Sodium Chloride, Sodium Lactate, Calcium Chloride, and Magnesium Chloride.
Target Population: Applicable for elderly, children, and adult patients.
Packaging Type: Non-PVC co-extruded film plastic infusion bag with double hose and double valve.
Quality Control: 100% visual and function inspection for all finished products.
Certification: ISO9001:2015 management system certified manufacturer.
Customization Service: Offers OEM, ODM, and flexible customization from samples or designs.
Company profile
CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc. CertifiedExport Year: 25 Years CertifiedNearest Port: Qingdao PortAverage Response Time: >24h
AI-Powered supplier vetting
SummaryThe supplier is a limited company founded in 1998, with 559 employees and a 54,736.0 m² manufacturing plant. It operates across pharmaceuticals, APIs, medical devices, medical services, medical supplies, and related production and trading activities. Evidence confirms OEM services for well-known brands, SDK availability, valid manufacturing contracts, quality assurance, raw-material traceability, and documented corrective-action and complaint-handling procedures. The supplier has an effective import/export license and reports overseas service coverage in Russia, but lacks in-stock capacity, overseas warehouses, overseas showrooms, overseas agents or branches, and offline trade-show participation. Financial information is insufficient for a credibility assessment, and no specific customer cases or formal certifications are provided.
Supplier typeThe supplier is identified as a limited company and a combined business, founded in 1998, with activities spanning pharmaceutical and health products, medical devices, manufacturing, processing, and sales. It is not identified as an offshore company and is not part of a larger company group.
After-Sales capabilityThe supplier has documented corrective and preventive action procedures, complaint-handling procedures with records, quality assurance, and raw-material traceability. It can provide overseas services in Russia, but has no overseas agents or branches, overseas warehouse, or overseas showroom, limiting local and inventory-based support.
R&D capabilityThe supplier explicitly reports R&D capability and SDK availability, and describes a strategy involving independent research and collaborative innovation. Its company profile also states that it integrates R&D, production, and sales, supporting a positive assessment of innovation capability.
Production capacityThe supplier operates a 54,736.0 m² manufacturing plant, has 559 employees, and covers pharmaceutical, API, medical-device, medical-supply, textile, and protective-product production activities. Valid manufacturing contracts exist with each related subcontractor, although the supplier reports no in-stock service capacity.
Customization capabilityOEM service for well-known brands is explicitly confirmed, indicating the ability to manufacture according to customer or brand requirements. The supplier also has documented service-capability assessment procedures and 30 qualified service suppliers, but no further details on product-development customization scope are provided.
Product Q&A
Q:What is the validity period of the product?
A:
The validity period is 24 months.
Q:What are the available glucose concentrations?
A:
Available concentrations include 1.5% and 2.5% Glucose peritoneal dialysis solution.
Q:What is the packaging material?
A:
It uses a non-PVC co-extruded film plastic infusion bag with a double hose, double valve, and double plug.
Q:Is OEM or ODM service available?
A:
Yes, the manufacturer offers OEM, ODM, and flexible customization services.
Q:What is the lead time for orders?
A:
Peak season lead time is one month, while off-season lead time is within 15 workdays.
Send Inquiry
*To:
Huaren Pharmaceutical Co., Ltd.
Huaren Pharmaceutical Co., Ltd.*Content:
Supplier replies will be sent to your registered email
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