What is the active ingredient content?

The active ingredient is 24%-28% (W/V) Citric Acid Solution.

What are the available net contents?

Available sizes include 600ml/bottle, 2.5L/bottle, and 5L/barrel.

Medical Disinfectant 20% Citric Acid Solution for Hemodialysis Machine

Name: Medical Disinfectant 20% Citric Acid Solution for Hemodialysis Machine
Brand: Shandong Retouch Wash and Sterilize Technology Co., Ltd.
SKU: 2029005112

Shandong, ChinaShandong Retouch Wash and Sterilize Technology Co., Ltd.

US$10.00

100 Pieces

Sample price:US$10.00/piece.Request sample

Product profile

Customization

Available

Usage

Medical Consumables

Type

Citric Acid Solution

Effect

Efficient

Active Ingredient

24-28% Citric Acid

Uses

Hospital

Net Content

Certificate

ISO9001,MSDS

Forms

Liquid

Transport Package

Bottles in Carton

Specification

5L/barrel

Trademark

Retouch

Origin

China

HS Code

3808940010

Production Capacity

30000pieces/Day

Key features

Super Cleaning Ability: Removes organic matter and calcium deposits, protecting inner rubber components.

OEM/ODM Service: We provide customized designs and packaging services for clients.

ISO9001 Certified: Passed ISO9001:2008 quality management system certification.

Professional Manufacturer: Founded in 2001, specializing in R&D and manufacturing of disinfection products.

Global Export Experience: Products exported to EU, Asia Pacific, and African countries.

Flexible MOQ: MOQ depends on material; lower for stock or existing designs.

Quality Guarantee: 100% responsibility for product quality issues.

Company profile

High Repeat Buyers ChoiceImporters and ExportersSelf-brandedNational Award received

Shandong Retouch Wash and Sterilize Technology Co., Ltd.

Shandong, China

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: 7 Years CertifiedNearest Port: Qingdao PortAverage Response Time: ≤8.84h

AI-Powered supplier vetting

SummaryThe supplier operates in medical devices, hygiene products, disinfectants, personal hygiene products, and related import/export activities. It reports production and sales capabilities covering Class I–III medical devices, although the provided business-scope records include both licensed and general project descriptions that should be verified. The supplier has documented procedures for complaints, corrective and preventive actions, finished-product inspection, and supplier assessment. It offers extensive customization and ODM/OEM services, holds CE-related certification, and has an available SDK. Export activity has continued for seven years, with self-operated import/export rights and stated peak- and off-season lead times within 15 working days. However, it reports no overseas warehouse or showroom, no new product in the past year, no Fortune 500 cooperation, and only five R&D engineers. Financial records are referenced for multiple years, but the slices provide no performance figures.

Supplier typeThe supplier’s stated scope covers medical-device production and sales, hygiene and disposable medical products, disinfectants, personal hygiene products, hazardous-chemical operations, and import/export activities. The records include Class I–III medical-device activities, but the exact current authorization status should be verified because the scope entries distinguish licensed projects from general projects.

CertificationsThe supplier reports CE certification for product compliance and sustainable development/product certification capability, along with other management-system and raw-material-report certifications. CE is explicit, while the unspecified “Others” entries do not identify additional standards or certification names.

After-Sales capabilityThe supplier has clear procedures and followed records for corrective and preventive actions and customer complaints, plus written and followed procedures for finished-product inspection and supplier-service assessment. These records support an organized service and quality-response process, although no specific response-time or resolution-performance metrics are provided.

Production capacityProduction capability is supported by stated Class I–III medical-device activities, valid manufacturing contracts with associated subcontractors, in-stock capability, inspection instructions that are uniformly followed, 80 qualified service-capability suppliers, and lead times within 15 working days in both peak and off-season. The supplier lacks overseas warehouse and showroom capability, which limits geographic service infrastructure but does not negate its reported manufacturing capacity.

Customization capabilityThe supplier explicitly offers customization from samples, designs, full customization, minor customization, flexible customization, and ODM services. This indicates broad customization coverage across both customer-provided inputs and supplier-led design/manufacturing.

Client casesThe supplier reports OEM service for well-known brands and a repeat-buyer preference rate of 50%–80%, providing evidence of brand-serving and repeat-customer experience. It also explicitly reports no cooperation with Fortune 500 companies, and no named customer cases are supplied.