Premium Enzyme Cleaner for Automatic Endoscope Cleaning Machines

Name: Premium Enzyme Cleaner for Automatic Endoscope Cleaning Machines
Brand: Shandong Retouch Wash and Sterilize Technology Co., Ltd.
SKU: 2072791302

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

US$11.50

500 Pieces

Sample price:US$6.50/piece.Request sample

Product profile

Customization

Available

Type

Disinfectant

Term of Validity

24 Months

Model NO.

AD10088

Function

Endoscope Disinfection

Main Ingredients

Proteolytic Enzyme

OEM

Yes

Transport Package

Bottles in Carton

Specification

1L, 2.5L, 5L or customized

Trademark

Retouch

Origin

China

HS Code

3808940090

Production Capacity

20000 Bottles/Bottles Per Day

Key features

Multi-Enzyme Formula: Contains protease, lipase, amylase, and 30% Propylene Glycol for powerful cleaning.

Rapid Cleaning Action: Dissolves pollutants swiftly with a simple 2-minute soak in the diluent.

Low Foam Design: Super concentrated formula produces minimal foam for optimal performance.

Safe for Instruments: No corrosion or aging effects on precision instruments and medical equipment.

Eco-Friendly Composition: Free from VOCs and phosphates; fully biodegradable and adheres to ecological standards.

Versatile Application: Suitable for soft/hard endoscopes, surgical appliances, rubber, plastics, and lab utensils.

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

Certified Quality: ISO9001:2008 certified with advanced independent laboratory testing capabilities.

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: ≤8.44h

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.