Raw Material Nad Ghk-Cu Glutathione Nad+

Name: Raw Material Nad Ghk-Cu Glutathione Nad+
Brand: Changzhou KEALOR International Co., Ltd.
SKU: 2283563375

Jiangsu, ChinaChangzhou KEALOR International Co., Ltd.

US$30.00-120.00

1 Piece

Product profile

Customization

Available

Disposable

Pharmaceutical Technology

Chemical Synthesis

Model NO.

nad

Name

Meso Nano Needle

Sterilization

Properties

Pencil Point Spinal Needle

Certificate

CE ISO FDA

Effect

Anti-Aing

Appearance

Vial Freeze-Dried Powder

Storage

Cool and Dry Place, Room Temperature

Specific Usage

for Biological Purpose, Technical Grade

Purity

99%

Production Capacity 300000000

Certification

GMP, Hse, ISO 9001, USP, Bp

Solubility

DMSO (Slightly), Water (Slightly)

Fusing Point

>182°C (DEC.)

Type

Pharmaceutical Intermediates

Test Method

HPLC, Janoshik

Transport Package

Blister Package

Specification

2mg 5mg 10mg 15mg 50mg 60mg 100mg 500mg

Trademark

KEALOR

Origin

China

HS Code

300120001

Production Capacity

50000kits/Month

Company profile

High Repeat Buyers ChoiceQuality AssuranceRaw-Materials TraceabilityQA/QC Inspectors

Changzhou KEALOR International Co., Ltd.

Jiangsu, China

Business Type: Manufacturer/FactoryExport Year: 2025-02-18Nearest Port: shanghaiAverage Response Time: ≤15hTerms of Payment: LC, T/T, D/P, etc.International Commercial Terms(Incoterms): FOB, EXW, CFR, CIF, DAT, FAS, DDP, DAP, CIP, CPT, Others, FCA

AI-Powered supplier vetting

SummaryKealor presents evidence of established medical and aesthetic manufacturing capabilities, holding ISO 13485, ISO 9001, and GMP certifications, reporting 50 quality-control staff, annual output above the stated threshold, and experience supplying well-known brands. It offers OEM, ODM, and multiple customization options, with raw-material traceability and documented inspection instructions. However, the evidence is inconsistent regarding technical resources: one slice identifies only one R&D engineer and no quality-control test equipment, while another reports 11–20 years of total R&D engineer experience. The supplier lacks 3D software, SDK, overseas warehouses, overseas showrooms, overseas agents or branches, and offline trade-show participation. After-sales technical support is indicated, but formal service-management procedures are absent. Financial records are referenced for several years, but the provided data does not disclose financial performance details. Customer cases are not specifically identified.

Supplier typeThe supplier is explicitly described as not being a professional technical supplier, while its company description focuses on solutions for medical and aesthetic applications. Its certifications and manufacturing indicators support classification as a medical/aesthetic product manufacturer rather than a dedicated technical-services provider.

CertificationsThe supplier reports holding ISO 13485, ISO 9001, and GMP certifications. These explicitly demonstrate certifications covering medical-device quality management, general quality management, and good manufacturing practices.

Production capacityProduction-related evidence includes annual output above the stated threshold, in-stock capability, raw-material traceability, one quality-control inspector, random finished-product inspection, and inspection instructions that are uniformly followed. The supplier has no quality-control test equipment reported in one slice, and manufacturing-contract status is unknown, so production scale is demonstrated but process depth and capacity assurance are only partially evidenced.

Customization capabilityThe supplier explicitly offers customization from samples, customization from designs, full customization, minor customization, and flexible customization, together with OEM and ODM services. These repeated capabilities indicate broad product customization support, despite the absence of 3D software design services.