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Hemorheological Testing Additive Heparin Lithium White Powder with Good Water Solubility
US$1.50
25 kg
Product profile
Customization
AvailableCAS No.
9045-22-1Formula
(C14h25no20s3)N.XliModel NO.
Heparin LithiumEINECS
NonAppearance
PowderUsage
Blood Collection Tubes AdditivesColor
WhiteOEM Packing
YesSafety
YesAnticoagulant
YesPurity
Above 99%Primitive Trait
White Amorphous PowderPerformance
Odorless, Soluble in Water, Easily HyPotency
Greater Than 150iu/MgAverage Molecular Weight
15000Valid Period
3 YearsTransport Package
BottleSpecification
10g/bottle; 50g/bottleTrademark
DeshengOrigin
ChinaHS Code
29319090Key features
High Potency: Potency is greater than 150IU/mg, ensuring effective anticoagulation performance.
Excellent Solubility: White amorphous powder that is odorless and easily soluble in water.
Long Validity Period: Product remains stable for 3 years when stored in cool and dry conditions.
Low Ion Interference: Ideal for determining blood ions as it causes the least interference.
Customizable Packaging: Available in 10g, 20g, and 50g bottles to meet various needs.
OEM Service Available: Customization from samples and OEM packing options are supported.
Stable at Room Temperature: Maintains stability under standard room temperature storage conditions.
Versatile Application: Suitable for clinical biochemical, emergency, and hemorheology blood tests.
Company profile
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 PortAverage Response Time: ≤7.25h
AI-Powered supplier vetting
SummaryThe supplier is a combined manufacturing and trading enterprise with chemical, synthetic-material, medical-device, and related product activities. It reports two production lines, specified annual capacities for several products, finished-product inspection instructions, inventory capability, and an off-peak lead time within 15 working days. Service processes for corrective and preventive actions and customer complaints are documented and followed. R&D personnel provide technical support, with design and verification records available for audit, but no SDK is available. The supplier provides OEM services for well-known brands and can customize from samples. Limitations include no valid manufacturing-capacity contract with related subcontractors, no overseas warehouse, showroom, agent, or branch, and no stated overseas service countries. No explicit certification holdings or customer case details are provided.
Supplier typeThe supplier’s stated scope covers manufacturing of basic chemical raw materials, synthetic and bio-based materials, special chemical products, sealing fillers, engineering plastics, and Category I and Category II medical-device sales. It is identified as a combined company rather than an offshore company, indicating a mixed manufacturing and commercial operating model.
After-Sales capabilityThe supplier has documented and followed procedures for corrective and preventive actions and customer complaints, and technology engineers provide technical support for production and after-sales service. However, it reports no overseas agents or branches, no overseas warehouse or showroom, and zero stated countries for overseas services, limiting evidence of local international support.
R&D capabilityR&D engineers are responsible for R&D and technical support, and relevant design input, output, review, verification, and validation documents are available for audit. The supplier reports software-instrument capability using MestReNova, but no SDK is available, so the evidence supports established R&D activity rather than full software-development integration capability.
Production capacityThe supplier operates two production lines and reports defined annual capacities, including 600 tons of serum separation gel, 500 tons of tris base, 30 tons of dipotassium ethylenediaminetetraacetate, 20 tons of tripotassium EDTA, and 0.6 tons of lithium heparin. It also reports inventory capability, standardized finished-product inspection instructions, and an off-peak lead time within 15 working days; however, it lacks a valid manufacturing-capacity contract with related subcontractors.
Customization capabilityThe supplier explicitly offers design customization from samples and reports OEM services for well-known brands. Its quality-control information also states that own-brand product quality-control capability is present, although the specific designation is recorded as “DS.”
Product Q&A
Q:Who are we?
A:
We are Hubei Xindesheng Material Technology Co., Ltd., a professional manufacturer of in vitro diagnostic reagent raw materials.
Q:Where is the company?
A:
Huarong District, Ezhou City, Hubei Province, is adjacent to Wuhan City. Welcome to visit the company!
Q:What is the delivery time?
A:
It is determined based on the inventory status of the product and the production and delivery status on that day. Generally, if there is stock available, shipment will be arranged on the day of placing the order.
Q:How to choose the transportation method?
A:
Determine based on the urgency of the customer's purchase of products and needs. When the quantity of products is low and the value is high, it is recommended to choose air freight or international express delivery; When there is a large quantity of products, choosing sea or land transportation is more cost-effective.
Q:What are the payment methods available?
A:
T/T, LC, etc.
Send Inquiry
*To:
Hubei New Desheng Material Technology Co., Ltd
Hubei New Desheng Material Technology Co., Ltd*Content:
Supplier replies will be sent to your registered email
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