Can this product be used with separation gel?

Yes, sodium heparin can be used simultaneously with separation gel to obtain high-quality plasma samples.

Sodium Heparin Testting Method Blood Anticoagulant Tubes Additives Chemical Reagent

Name: Sodium Heparin Testting Method Blood Anticoagulant Tubes Additives Chemical Reagent
Brand: Hubei New Desheng Material Technology Co., Ltd
SKU: 2065042775

Hubei, ChinaHubei New Desheng Material Technology Co., Ltd

US$1.50

25 kg

Product profile

Customization

Available

CAS No.

9041-08-1

Formula

(C14h25no20s3)N.Xna

Model NO.

Heparin Sodium

EINECS

Non

Appearance

Powder

Usage

Blood Collection Tubes Additives

Color

White

OEM Packing

Yes

Purity

High

Validity

3 Years

Dangerous

Valid Period

3 Years

Potency

Over 150iu/Mg

pH Value

5.0-7.5

Clarity of Solution

Colorless Clarification

Transport Package

Bottle

Specification

10g/bottle, 50g/bottle

Trademark

Desheng

Origin

China

HS Code

30019010

Key features

Blood Anticoagulant: Ideal for clinical biochemical and emergency blood sample collection with minimal ion interference.

OEM Packing: Customized packaging options available for bulk orders.

Long Validity: Product validity period is 3 years when stored correctly.

Stable Formulation: White amorphous powder, odorless, soluble in water, and stable at room temperature.

Versatile Application: Suitable for hemorheology projects and ion content determination in clinical tests.

Compatible with Gel: Can be used simultaneously with separation gel for high-quality plasma samples.

Manufacturer Direct: Produced by Hubei New Desheng with professional R&D team and advanced equipment.

Company profile

Importers and ExportersPatents AwardedExhibition Experience

Hubei New Desheng Material Technology Co., Ltd

Hubei, 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 PortAverage Response Time: ≤8.94h

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.”