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Biochemical Reagent Ingredients Vacuum Plasma Separator Te Serum Separating Gel

Name: Biochemical Reagent Ingredients Vacuum Plasma Separator Te Serum Separating Gel
Brand: Hubei New Desheng Material Technology Co., Ltd
SKU: 2074346845

Hubei, ChinaHubei New Desheng Material Technology Co., Ltd

US$1.50

25 kg

Product profile

Customization

Available

CAS No.

Non

Formula

Non

Model NO.

Serum Separating Gel

EINECS

Non

Appearance

Gel

Usage

Blood Collection Tubes Additives

Color

Transparent

Other Color

Transparent, Semi Transparent, Opaque

Packing Specification

20kg/Barrel, 25kg/Barrel

Validity

36 Months

Factory Supply

Yes

Viscosity

100000 to 300000 Kpa

Relative Specific Gravity

1.045-1.065g/cm3

Water Solubility

Insoluble in Water

Volatile

Less Than 1.5%

Transport Package

25kg/Barrel

Specification

25kg

Trademark

Desheng

Origin

China

HS Code

2942000000

Key features

Patented Unique Composition: Proprietary formula ensures high purity and performance without mixing with other suppliers.

Excellent Thixotropic Properties: Provides superior isolation and stability for serum separation in vacuum blood collection tubes.

High Vacuum Treatment: Processed to remove almost all air, preventing bubble formation and ensuring accurate dispensing.

Physiologically Inert: Safe, non-toxic, and insoluble in water, making it ideal for clinical blood sample storage.

Customizable Specifications: Available in various colors (Transparent, Semi-Transparent, Opaque) and packing sizes (20kg/25kg).

Professional Manufacturer: Produced by Hubei New Desheng with 9 R&D engineers and advanced production 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: ≤6.02h

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.”